A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701301



Internal ID15437953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16773509..16775341hg38UCSC Ensembl
Innerchr22:17254399..17256231hg19UCSC Ensembl
Innerchr22:15634399..15636231hg18UCSC Ensembl
Innerchr22:15628953..15630785hg17UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg381833
hg191833
hg181833
hg171833
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517059
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701301
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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