A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521052



Internal ID15448345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43043646..43047034hg38UCSC Ensembl
Innerchr7:43083245..43086633hg19UCSC Ensembl
Innerchr7:43049770..43053158hg18UCSC Ensembl
Innerchr7:42856485..42859873hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383389
hg193389
hg183389
hg173389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697755
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521052
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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