A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590850



Internal ID16378259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84477262..84581154hg38UCSC Ensembl
Innerchr3:84526413..84630305hg19UCSC Ensembl
Innerchr3:84609103..84712995hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38103893
hg19103893
hg18103893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152489
Samples1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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