A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592159



Internal ID16379568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162395328..162459502hg38UCSC Ensembl
Innerchr3:162113116..162177290hg19UCSC Ensembl
Innerchr3:163595810..163659984hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3864175
hg1964175
hg1864175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8667n54
Supporting Variantsnssv977370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592159
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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