A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428862



Internal ID22486732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99125886..99225484hg38UCSC Ensembl
chr5:98461590..98561188hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3899599
hg1999599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428862
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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