A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939677



Internal ID27170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136709000..136714000hg38UCSC Ensembl
chr3:136427842..136432842hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451678
Supporting Variants
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939677
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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