A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698551



Internal ID15435203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91494107..91581358hg38UCSC Ensembl
Innerchr7:91123422..91210673hg19UCSC Ensembl
Innerchr7:90961358..91048609hg18UCSC Ensembl
Innerchr7:90768073..90855324hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3887252
hg1987252
hg1887252
hg1787252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522893
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698551
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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