A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679514



Internal ID15069480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126497978..126505786hg38UCSC Ensembl
Innerchr9:129260257..129268065hg19UCSC Ensembl
Innerchr9:128300078..128307886hg18UCSC Ensembl
Innerchr9:126339811..126347619hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387809
hg197809
hg187809
hg177809
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)nssv679514
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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