A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590199



Internal ID16030922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46756643..46805202hg38UCSC Ensembl
Innerchr3:46798133..46846692hg19UCSC Ensembl
Innerchr3:46773137..46821696hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3848560
hg1948560
hg1848560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8304n54
Supporting Variantsnssv962589, nssv962590, nssv962581, nssv962582, nssv962583, nssv962584, nssv962585, nssv962591, nssv962586, nssv962587, nssv962588
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590199
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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