A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891139



Internal ID19185535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:68639201..68660416hg38UCSC Ensembl
Outerchr7:68639201..68660416hg38UCSC Ensembl
Innerchr7:68104188..68125403hg19UCSC Ensembl
Outerchr7:68104188..68125403hg19UCSC Ensembl
Innerchr7:67742124..67763339hg18UCSC Ensembl
Outerchr7:67742124..67763339hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3821216
hg1921216
hg1821216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784634
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891139
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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