A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657995



Internal ID15394647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47826296..47840491hg38UCSC Ensembl
Innerchr22:48222045..48236240hg19UCSC Ensembl
Innerchr22:46600709..46614904hg18UCSC Ensembl
Innerchr22:46542564..46556759hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3814196
hg1914196
hg1814196
hg1714196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519733
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657995
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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