A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015220



Internal ID21924563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173068970..173073556hg38UCSC Ensembl
chr5:172495973..172500559hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg384587
hg194587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559466
Samples
Known GenesCREBRF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015220
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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