A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891200



Internal ID19185596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124990785..126688176hg38UCSC Ensembl
Outerchr7:124990785..126688176hg38UCSC Ensembl
Innerchr7:124630839..126328230hg19UCSC Ensembl
Outerchr7:124630839..126328230hg19UCSC Ensembl
Innerchr7:124418075..126115466hg18UCSC Ensembl
Outerchr7:124418075..126115466hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg381697392
hg191697392
hg181697392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783439
Samples
Known GenesGRM8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891200
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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