A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604792



Internal ID21796839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37280744..37280744hg38UCSC Ensembl
chr13:37854881..37854881hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604792
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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