A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692358



Internal ID18643953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2233969..2364269hg38UCSC Ensembl
Innerchr9:2233969..2364269hg19UCSC Ensembl
Innerchr9:2223969..2354269hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38130301
hg19130301
hg18130301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029947
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)nssv3692358
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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