A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009736



Internal ID74138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41805065..41810627hg38UCSC Ensembl
chr8:41662583..41668145hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385563
hg195563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491781
Supporting Variants
Samples
Known GenesANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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