A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546061



Internal ID16333470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38669208..38706616hg38UCSC Ensembl
Innerchr1:39134880..39172288hg19UCSC Ensembl
Innerchr1:38907467..38944875hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3837409
hg1937409
hg1837409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173815
SamplesHGDP00157
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546061
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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