A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038457



Internal ID93368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100247808..100248329hg38UCSC Ensembl
chr10:102007565..102008086hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484206
Supporting Variants
Samples
Known GenesCWF19L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038457
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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