A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688566



Internal ID15078532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126497978..126503862hg38UCSC Ensembl
Innerchr9:129260257..129266141hg19UCSC Ensembl
Innerchr9:128300078..128305962hg18UCSC Ensembl
Innerchr9:126339811..126345695hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385885
hg195885
hg185885
hg175885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516074
Supporting Variants
Samples
Known GenesMVB12B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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