A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951159



Internal ID34797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57137232..57156261hg38UCSC Ensembl
chr4:58003398..58022427hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3819030
hg1919030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455590
Supporting Variants
Samples
Known GenesIGFBP7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951159
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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