A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700790



Internal ID15437442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44215170..44221984hg38UCSC Ensembl
Innerchr22:44611050..44617864hg19UCSC Ensembl
Innerchr22:42942383..42949197hg18UCSC Ensembl
Innerchr22:42935951..42942765hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg386815
hg196815
hg186815
hg176815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524798
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700790
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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