A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546455



Internal ID15987178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70415034..70421500hg38UCSC Ensembl
Innerchr1:70880717..70887183hg19UCSC Ensembl
Innerchr1:70653305..70659771hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg386467
hg196467
hg186467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv716148
Samples
Known GenesCTH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546455
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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