A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989214



Internal ID60236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159816126..159816140hg38UCSC Ensembl
chr6:160237158..160237172hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542717
Supporting Variants
Samples
Known GenesPNLDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989214
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.445984


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