A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677816



Internal ID15067782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:19974680..19985682hg38UCSC Ensembl
Innerchr22:19962203..19973205hg19UCSC Ensembl
Innerchr22:18342203..18353205hg18UCSC Ensembl
Innerchr22:18336757..18347759hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3811003
hg1911003
hg1811003
hg1711003
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517165
Supporting Variants
Samples
Known GenesARVCF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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