A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760848



Internal ID19059129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61619207hg38UCSC Ensembl
Innerchr9:44727847..44827045hg19UCSC Ensembl
Innerchr9:44667843..44767041hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3899199
hg1999199
hg1899199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030799
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)nssv3760848
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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