A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542802



Internal ID21867157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39333608..39333608hg38UCSC Ensembl
chr5:39333710..39333710hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076705
Supporting Variants
Samples
Known GenesC9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542802
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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