A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591371



Internal ID16378780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632551..119635586hg38UCSC Ensembl
Innerchr3:119351398..119354433hg19UCSC Ensembl
Innerchr3:120834088..120837123hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383036
hg193036
hg183036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8519n54
Supporting Variantsnssv971714, nssv971711, nssv971713, nssv971710, nssv971715, nssv971716, nssv971712
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591371
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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