A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755913



Internal ID19054194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30419932..30560431hg38UCSC Ensembl
Innerchr9:30419930..30560429hg19UCSC Ensembl
Innerchr9:30409930..30550429hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38140500
hg19140500
hg18140500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029183
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)nssv3755913
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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