A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545402



Internal ID15986125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10630891..10736809hg38UCSC Ensembl
Innerchr1:10690948..10796866hg19UCSC Ensembl
Innerchr1:10613535..10719453hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38105919
hg19105919
hg18105919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv105n54
Supporting Variantsnssv1173668
Samples1780862093_A
Known GenesCASZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545402
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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