A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951824



Internal ID35245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92888400..93056297hg38UCSC Ensembl
chr4:93809551..93977448hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38167898
hg19167898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454897
Supporting Variants
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951824
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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