A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643617



Internal ID21835664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118031482..118031482hg38UCSC Ensembl
chrX:117165445..117165445hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042691
Supporting Variants
Samples
Known GenesKLHL13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643617
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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