A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570548



Internal ID21762591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112394525..112399577hg38UCSC Ensembl
chr6:112715727..112720779hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385053
hg195053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570548
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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