A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696494



Internal ID15433146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86572060..86573375hg38UCSC Ensembl
Innerchr9:89186975..89188290hg19UCSC Ensembl
Innerchr9:88376795..88378110hg18UCSC Ensembl
Innerchr9:86416529..86417844hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381316
hg191316
hg181316
hg171316
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519025
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696494
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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