A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893764



Internal ID19184584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113761834..113787887hg38UCSC Ensembl
Outerchr3:113761834..113787887hg38UCSC Ensembl
Innerchr3:113480681..113506734hg19UCSC Ensembl
Outerchr3:113480681..113506734hg19UCSC Ensembl
Innerchr3:114963371..114989424hg18UCSC Ensembl
Outerchr3:114963371..114989424hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3826054
hg1926054
hg1826054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779354
Samples
Known GenesATP6V1A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893764
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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