A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525104



Internal ID15105711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80361713..80372907hg38UCSC Ensembl
Innerchr7:79991029..80002223hg19UCSC Ensembl
Innerchr7:79828965..79840159hg18UCSC Ensembl
Innerchr7:79635680..79646874hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3811195
hg1911195
hg1811195
hg1711195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701163
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525104
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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