A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531295



Internal ID21855651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227574496..227574496hg38UCSC Ensembl
chr1:227762197..227762197hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054844
Supporting Variants
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531295
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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