A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424675



Internal ID22482545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13513076..13515811hg38UCSC Ensembl
chr5:13513186..13515921hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382736
hg192736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424675
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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