A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630460



Internal ID21822507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41633212..41633212hg38UCSC Ensembl
chr17:39789464..39789464hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091702
Supporting Variants
Samples
Known GenesKRT42P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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