A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678216



Internal ID21200072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32581183..32581183hg38UCSC Ensembl
chr1:33046784..33046784hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801926
Supporting Variants
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678216
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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