A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903895



Internal ID3415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63292030..63292434hg38UCSC Ensembl
chr1:63757701..63758105hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432494
Supporting Variants
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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