A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002584



Internal ID18745116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196008062..196183901hg38UCSC Ensembl
Innerchr3:195734933..195910772hg19UCSC Ensembl
Innerchr3:197219330..197395169hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38175840
hg19175840
hg18175840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616992
Samples
Known GenesLINC00885, TFRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002584
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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