A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545404



Internal ID15986127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10697142..10736809hg38UCSC Ensembl
Innerchr1:10757199..10796866hg19UCSC Ensembl
Innerchr1:10679786..10719453hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3839668
hg1939668
hg1839668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173669
Samples1780862416_A
Known GenesCASZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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