A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604690



Internal ID21796737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26559788..26559788hg38UCSC Ensembl
chr13:27133925..27133925hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087700
Supporting Variants
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604690
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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