A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690736



Internal ID18989017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23326891..23410598hg38UCSC Ensembl
Innerchr9:23326889..23410596hg19UCSC Ensembl
Innerchr9:23316889..23400596hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3883708
hg1983708
hg1883708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026141
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690736
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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