A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534834



Internal ID21859189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11829560..11829560hg38UCSC Ensembl
chr1:11889617..11889617hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057051
Supporting Variants
Samples
Known GenesCLCN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534834
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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