A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592156



Internal ID16379565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162378607..162424687hg38UCSC Ensembl
Innerchr3:162096395..162142475hg19UCSC Ensembl
Innerchr3:163579089..163625169hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3846081
hg1946081
hg1846081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8665n54
Supporting Variantsnssv1153399
SamplesNINDS_183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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