A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735291



Internal ID158957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150106465..150114456hg38UCSC Ensembl
chr6:150427601..150435592hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387992
hg197992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735291
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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