A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590632



Internal ID16378041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72909726..72987471hg38UCSC Ensembl
Innerchr3:72958877..73036622hg19UCSC Ensembl
Innerchr3:73041567..73119312hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3877746
hg1977746
hg1877746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965591
Samples
Known GenesGXYLT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590632
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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