A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945946



Internal ID31305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195159906..195160943hg38UCSC Ensembl
chr3:194880635..194881672hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444030
Supporting Variants
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945946
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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