A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546019



Internal ID16333428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38136401..38138415hg38UCSC Ensembl
Innerchr1:38602073..38604087hg19UCSC Ensembl
Innerchr1:38374660..38376674hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382015
hg192015
hg182015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv235n54
Supporting Variantsnssv712366
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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