A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713269



Internal ID136935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44042690..44045153hg38UCSC Ensembl
chr17:42120058..42122521hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382464
hg192464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529280
Supporting Variants
Samples
Known GenesLSM12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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