A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527462



Internal ID15454755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50865673..50921686hg38UCSC Ensembl
Innerchr7:50933370..50989383hg19UCSC Ensembl
Innerchr7:50900864..50956877hg18UCSC Ensembl
Innerchr7:50707579..50763592hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3856014
hg1956014
hg1856014
hg1756014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703905
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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