A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036039



Internal ID91767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49114257..49130180hg38UCSC Ensembl
chr10:50322302..50338225hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3815924
hg1915924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488820
Supporting Variants
Samples
Known GenesFAM170B-AS1, VSTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036039
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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