A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977922



Internal ID52683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121400..296000hg38UCSC Ensembl
chr6:121400..296000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38174601
hg19174601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140819
Supporting Variants
Samples
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977922
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000626


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer