A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908801



Internal ID6654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:107867455..107867511hg38UCSC Ensembl
chr1:108410077..108410133hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422717
Supporting Variants
Samples
Known GenesVAV3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908801
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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