A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655392



Internal ID15392044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113642423..113644627hg38UCSC Ensembl
Innerchr9:116404703..116406907hg19UCSC Ensembl
Innerchr9:115444524..115446728hg18UCSC Ensembl
Innerchr9:113484257..113486461hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382205
hg192205
hg182205
hg172205
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655392
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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