A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419357



Internal ID22477227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102752761..102753108hg38UCSC Ensembl
chr5:102088465..102088812hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419357
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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