A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544112



Internal ID21868467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70336793..70336793hg38UCSC Ensembl
chr4:71202510..71202510hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069649
Supporting Variants
Samples
Known GenesCABS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544112
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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