A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592177



Internal ID16379586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162412903..162520451hg38UCSC Ensembl
Innerchr3:162130691..162238239hg19UCSC Ensembl
Innerchr3:163613385..163720933hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38107549
hg19107549
hg18107549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8673n54
Supporting Variantsnssv1152026
SamplesNINDS_216
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592177
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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