A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696944



Internal ID15433596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39175429..39190092hg38UCSC Ensembl
Innerchr22:39571434..39586097hg19UCSC Ensembl
Innerchr22:37901380..37916043hg18UCSC Ensembl
Innerchr22:37895934..37910597hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3814664
hg1914664
hg1814664
hg1714664
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519600
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696944
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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