A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690562



Internal ID18988843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12023071..12227078hg38UCSC Ensembl
Innerchr9:12023071..12227078hg19UCSC Ensembl
Innerchr9:12013071..12217078hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38204008
hg19204008
hg18204008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020196
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)nssv3690562
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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