A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680579



Internal ID15070545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113096943..113103737hg38UCSC Ensembl
Innerchr9:115859223..115866017hg19UCSC Ensembl
Innerchr9:114899044..114905838hg18UCSC Ensembl
Innerchr9:112938777..112945571hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386795
hg196795
hg186795
hg176795
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515822
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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