A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635665



Internal ID7022463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105863696..106714895hg38UCSC Ensembl
Innerchr14:105864196..106714395hg38UCSC Ensembl
Outerchr14:105862696..106715895hg38UCSC Ensembl
chr14:106329906..107170142hg19UCSC Ensembl
Innerchr14:106330406..107169642hg19UCSC Ensembl
Outerchr14:106328906..107171142hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38851200
hg19840237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15120154, essv15120159, essv15120157, essv15120158, essv15120156, essv15120160, essv15120155, essv15120161
SamplesNA18625, HG03212, HG01767, NA18573, NA19000, NA21143, NA19834, HG03886
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635665
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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