A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560920



Internal ID21885275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46996243..46998191hg38UCSC Ensembl
chr6:46963980..46965928hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381949
hg191949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560920
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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