A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713186



Internal ID136852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41422593..41422807hg38UCSC Ensembl
chr17:39578845..39579059hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556761
Supporting Variants
Samples
Known GenesKRT37
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713186
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.148923


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