A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426376



Internal ID22484246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41603888..41604209hg38UCSC Ensembl
chr5:41603990..41604311hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426376
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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