A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643733



Internal ID6683803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14042961..14045862hg38UCSC Ensembl
Innerchr19:14042999..14045824hg38UCSC Ensembl
Outerchr19:14042923..14045900hg38UCSC Ensembl
chr19:14153773..14156674hg19UCSC Ensembl
Innerchr19:14153811..14156636hg19UCSC Ensembl
Outerchr19:14153735..14156712hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382902
hg192902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15997189, essv15997195, essv15997192, essv15997191, essv15997194, essv15997196, essv15997193, essv15997190
SamplesHG02890, HG03279, HG02595, HG03397, HG02594, HG02586, NA20289, NA18864
Known GenesIL27RA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643733
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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