A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891122



Internal ID19185518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62519551..62962531hg38UCSC Ensembl
Outerchr7:62506780..63170073hg38UCSC Ensembl
Innerchr7:61979929..62422909hg19UCSC Ensembl
Outerchr7:61847454..62630451hg19UCSC Ensembl
Innerchr7:61617364..62060344hg18UCSC Ensembl
Outerchr7:61484889..62267886hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38663294
hg19782998
hg18782998
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789766, essv25790932, essv25788575
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891122
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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