A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704666



Internal ID15441318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2915463..2937133hg38UCSC Ensembl
Innerchr7:2955097..2976767hg19UCSC Ensembl
Innerchr7:2921623..2943293hg18UCSC Ensembl
Innerchr7:2728338..2750008hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3821671
hg1921671
hg1821671
hg1721671
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528122
Supporting Variants
Samples
Known GenesCARD11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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