A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591226



Internal ID16378635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104712743..104765548hg38UCSC Ensembl
Innerchr3:104431587..104484392hg19UCSC Ensembl
Innerchr3:105914277..105967082hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3852806
hg1952806
hg1852806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971244
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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