A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698166



Internal ID15434818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88106531..88141515hg38UCSC Ensembl
Innerchr9:90721446..90756430hg19UCSC Ensembl
Innerchr9:89911266..89946250hg18UCSC Ensembl
Innerchr9:87951000..87985984hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3834985
hg1934985
hg1834985
hg1734985
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521551
Supporting Variants
Samples
Known GenesSPATA31C2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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