A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3761469



Internal ID19059750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61665362hg38UCSC Ensembl
Innerchr9:44727847..44873200hg19UCSC Ensembl
Innerchr9:44667843..44813196hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38145354
hg19145354
hg18145354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035019
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)nssv3761469
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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