A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521512



Internal ID15448805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95448863..95448984hg38UCSC Ensembl
Innerchr7:95078175..95078296hg19UCSC Ensembl
Innerchr7:94916111..94916232hg18UCSC Ensembl
Innerchr7:94722826..94722947hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38122
hg19122
hg18122
hg17122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694455
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521512
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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