A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903699



Internal ID3285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35789176..35792097hg38UCSC Ensembl
chr1:36254777..36257698hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382922
hg192922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420976
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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