A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009583



Internal ID18752114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162111914..163202422hg38UCSC Ensembl
Innerchr3:161829702..162920210hg19UCSC Ensembl
Innerchr3:163312396..164402904hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381090509
hg191090509
hg181090509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606426
Samples
Known GenesCT64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009583
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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