A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659725



Internal ID15396377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12476544..12524502hg38UCSC Ensembl
Innerchr7:12516170..12564128hg19UCSC Ensembl
Innerchr7:12482695..12530653hg18UCSC Ensembl
Innerchr7:12289410..12337368hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3847959
hg1947959
hg1847959
hg1747959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519965
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659725
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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