A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525687



Internal ID15452980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124498133..124556390hg38UCSC Ensembl
Innerchr7:124138187..124196444hg19UCSC Ensembl
Innerchr7:123925423..123983680hg18UCSC Ensembl
Innerchr7:123732138..123790395hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3858258
hg1958258
hg1858258
hg1758258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701845
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525687
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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