A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702909



Internal ID15092875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25532653..25534512hg38UCSC Ensembl
Innerchr22:25928620..25930479hg19UCSC Ensembl
Innerchr22:24258620..24260479hg18UCSC Ensembl
Innerchr22:24253174..24255033hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381860
hg191860
hg181860
hg171860
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517205
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702909
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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