A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644897



Internal ID6684960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57195504..57202916hg38UCSC Ensembl
Innerchr19:57195519..57202902hg38UCSC Ensembl
Outerchr19:57195490..57202931hg38UCSC Ensembl
chr19:57706872..57714284hg19UCSC Ensembl
Innerchr19:57706887..57714270hg19UCSC Ensembl
Outerchr19:57706858..57714299hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg387413
hg197413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107132, essv16107142, essv16107129, essv16107121, essv16107144, essv16107161, essv16107145, essv16107168, essv16107163, essv16107150, essv16107166, essv16107169, essv16107146, essv16107138, essv16107136, essv16107122, essv16107160, essv16107152, essv16107131, essv16107140, essv16107125, essv16107154, essv16107137, essv16107123, essv16107124, essv16107139, essv16107135, essv16107165, essv16107148, essv16107159, essv16107149, essv16107162, essv16107171, essv16107170, essv16107155, essv16107128, essv16107126, essv16107156, essv16107157, essv16107147, essv16107130, essv16107158, essv16107127, essv16107143, essv16107134, essv16107151, essv16107141, essv16107167, essv16107153, essv16107133, essv16107164
SamplesHG03514, HG02614, HG01402, HG02852, HG03521, NA20346, NA19314, HG03069, HG02895, HG03074, HG03099, HG02485, HG02620, HG02054, NA18498, NA20287, HG02816, HG01242, HG03209, HG02561, NA19235, HG03225, NA19025, HG02882, HG03048, HG02879, HG02442, HG03120, NA19908, NA19247, HG03511, HG03088, NA19184, NA19391, NA19982, NA18879, HG02884, HG02585, HG01956, HG02772, HG01894, HG03103, HG03084, HG02971, HG03066, HG02768, HG02013, NA19116, HG02465, HG03072, HG03271
Known GenesZNF264
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644897
Frequency
Sample Size2504
Observed Gain0
Observed Loss51
Observed Complex0
Frequencyn/a


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