A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593069



Internal ID16033792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196049369..196180782hg38UCSC Ensembl
Innerchr3:195776240..195907653hg19UCSC Ensembl
Innerchr3:197260637..197392050hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38131414
hg19131414
hg18131414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv986886
Samples
Known GenesLINC00885, TFRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593069
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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