A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429448



Internal ID22487318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13587393..13589844hg38UCSC Ensembl
chr5:13587502..13589953hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382452
hg192452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902917
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429448
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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