A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545960



Internal ID16333369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32513637..32621451hg38UCSC Ensembl
Innerchr1:32979238..33087052hg19UCSC Ensembl
Innerchr1:32751825..32859639hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38107815
hg19107815
hg18107815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712150
Samples
Known GenesZBTB8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545960
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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