A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420687



Internal ID22478557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135898765..135898841hg38UCSC Ensembl
chr5:135234454..135234530hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420687
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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