A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527530



Internal ID15454823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:94703080..94751197hg38UCSC Ensembl
Innerchr7:94332392..94380509hg19UCSC Ensembl
Innerchr7:94170328..94218445hg18UCSC Ensembl
Innerchr7:93977043..94025160hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3848118
hg1948118
hg1848118
hg1748118
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703988
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527530
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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