A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545168



Internal ID16332577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:5223963..5245304hg38UCSC Ensembl
Innerchr1:5284023..5305364hg19UCSC Ensembl
Innerchr1:5183883..5205224hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3821342
hg1921342
hg1821342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708948
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545168
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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