A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703593



Internal ID127259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84748839..84748850hg38UCSC Ensembl
chr15:85292070..85292081hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534166
Supporting Variants
Samples
Known GenesZNF592
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703593
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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