A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713158



Internal ID136824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41109624..41132879hg38UCSC Ensembl
chr17:39265876..39289131hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3823256
hg1923256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528003
Supporting Variants
Samples
Known GenesKRTAP4-11, KRTAP4-12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713158
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001874


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