A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705979



Internal ID15095945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36800927..36802832hg38UCSC Ensembl
Innerchr22:37196971..37198876hg19UCSC Ensembl
Innerchr22:35526917..35528822hg18UCSC Ensembl
Innerchr22:35521471..35523376hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381906
hg191906
hg181906
hg171906
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522590
Supporting Variants
Samples
Known GenesPVALB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705979
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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