A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696511



Internal ID18994792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137275904..137361369hg38UCSC Ensembl
Innerchr9:140170356..140255821hg19UCSC Ensembl
Innerchr9:139290177..139375642hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3885466
hg1985466
hg1885466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037407
Supporting Variants
Samples
Known GenesEXD3, NRARP, TOR4A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696511
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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