A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758166



Internal ID19056447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10755356..11281192hg38UCSC Ensembl
Innerchr9:10755356..11281192hg19UCSC Ensembl
Innerchr9:10745356..11271192hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38525837
hg19525837
hg18525837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021035
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)nssv3758166
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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