A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891064



Internal ID19185460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14657672..14698545hg38UCSC Ensembl
Outerchr7:14657672..14698545hg38UCSC Ensembl
Innerchr7:14697297..14738170hg19UCSC Ensembl
Outerchr7:14697297..14738170hg19UCSC Ensembl
Innerchr7:14663822..14704695hg18UCSC Ensembl
Outerchr7:14663822..14704695hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3840874
hg1940874
hg1840874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789842
Samples
Known GenesDGKB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891064
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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