A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562043



Internal ID21886398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170267629..170267697hg38UCSC Ensembl
chr6:170576717..170576785hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562043
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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