A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698596



Internal ID15435248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89891589..89977044hg38UCSC Ensembl
Innerchr7:89520903..89606358hg19UCSC Ensembl
Innerchr7:89358839..89444294hg18UCSC Ensembl
Innerchr7:89165554..89251009hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3885456
hg1985456
hg1885456
hg1785456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522933
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698596
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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