A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590633



Internal ID16378042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72914618..72961905hg38UCSC Ensembl
Innerchr3:72963769..73011056hg19UCSC Ensembl
Innerchr3:73046459..73093746hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3847288
hg1947288
hg1847288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965592
Samples
Known GenesGXYLT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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