A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546021



Internal ID16333430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38136401..38138876hg38UCSC Ensembl
Innerchr1:38602073..38604548hg19UCSC Ensembl
Innerchr1:38374660..38377135hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382476
hg192476
hg182476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv235n54
Supporting Variantsnssv712370, nssv712368, nssv712369
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546021
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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