A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590977



Internal ID16378386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90263904..90345178hg38UCSC Ensembl
Innerchr3:90313054..90394328hg19UCSC Ensembl
Innerchr3:90395744..90477018hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3881275
hg1981275
hg1881275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8440n54
Supporting Variantsnssv967762
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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