A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418201



Internal ID22476071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73099437..73099732hg38UCSC Ensembl
chr5:72395264..72395559hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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