A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521676



Internal ID21846035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203839978..203839978hg38UCSC Ensembl
chr1:203809106..203809106hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053855
Supporting Variants
Samples
Known GenesZC3H11A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521676
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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