A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706085



Internal ID15442737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:346691..351793hg38UCSC Ensembl
Innerchr9:346691..351793hg19UCSC Ensembl
Innerchr9:336691..341793hg18UCSC Ensembl
Innerchr9:336691..341793hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg385103
hg195103
hg185103
hg175103
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515505
Supporting Variants
Samples
Known GenesDOCK8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706085
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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