A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690959



Internal ID18989240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88018..309054hg38UCSC Ensembl
Innerchr9:88018..309054hg19UCSC Ensembl
Innerchr9:78018..299054hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38221037
hg19221037
hg18221037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023234
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690959
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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