A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591215



Internal ID16378624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104468641..104697747hg38UCSC Ensembl
Innerchr3:104187485..104416591hg19UCSC Ensembl
Innerchr3:105670175..105899281hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38229107
hg19229107
hg18229107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv970945
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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