A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937965



Internal ID26029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114039715..114039715hg38UCSC Ensembl
chr3:113758562..113758562hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538934
Supporting Variants
Samples
Known GenesKIAA1407
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937965
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.006244


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