A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545128



Internal ID15985851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3630371..3700037hg38UCSC Ensembl
Innerchr1:3546935..3616601hg19UCSC Ensembl
Innerchr1:3536795..3606461hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3869667
hg1969667
hg1869667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708847
Samples
Known GenesTP73, WRAP73
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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