A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590161



Internal ID16377570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45356494..45365100hg38UCSC Ensembl
Innerchr3:45397986..45406592hg19UCSC Ensembl
Innerchr3:45372990..45381596hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388607
hg198607
hg188607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151768
SamplesHGDP01269
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590161
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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