A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524754



Internal ID21849112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11829610..11829610hg38UCSC Ensembl
chr1:11889667..11889667hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040742
Supporting Variants
Samples
Known GenesCLCN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524754
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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