A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695557



Internal ID18993838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61692688hg38UCSC Ensembl
Innerchr9:44727847..44900526hg19UCSC Ensembl
Innerchr9:44667843..44840522hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38172680
hg19172680
hg18172680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028921
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)nssv3695557
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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