A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560870



Internal ID21885225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136970329..136970329hg38UCSC Ensembl
chr6:137291467..137291467hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560870
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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