A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590077



Internal ID16377486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37938391..37944758hg38UCSC Ensembl
Innerchr3:37979882..37986249hg19UCSC Ensembl
Innerchr3:37954886..37961253hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386368
hg196368
hg186368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962195, nssv962196, nssv962192, nssv962180, nssv962188, nssv962178, nssv962186, nssv962191, nssv962198, nssv962193, nssv962194, nssv962187, nssv962197, nssv962185, nssv962182, nssv962184, nssv962190, nssv962181, nssv962179, nssv962183, nssv962189
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590077
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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