A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695806



Internal ID15432458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90080467..90106185hg38UCSC Ensembl
Innerchr7:89709781..89735499hg19UCSC Ensembl
Innerchr7:89547717..89573435hg18UCSC Ensembl
Innerchr7:89354432..89380150hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3825719
hg1925719
hg1825719
hg1725719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695806
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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