A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902121



Internal ID2206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41606044..41606932hg38UCSC Ensembl
chr1:42071715..42072603hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417898
Supporting Variants
Samples
Known GenesHIVEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902121
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007181


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