A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3688867



Internal ID18987148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32905789..32992665hg38UCSC Ensembl
Innerchr9:32905787..32992663hg19UCSC Ensembl
Innerchr9:32895787..32982663hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3886877
hg1986877
hg1886877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025585
Supporting Variants
Samples
Known GenesAPTX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3688867
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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