A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893596



Internal ID18837730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:960344..1040314hg38UCSC Ensembl
Outerchr3:960344..1040314hg38UCSC Ensembl
Innerchr3:1002028..1081998hg19UCSC Ensembl
Outerchr3:1002028..1081998hg19UCSC Ensembl
Innerchr3:977028..1056998hg18UCSC Ensembl
Outerchr3:977028..1056998hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3879971
hg1979971
hg1879971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778901
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893596
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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