A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126708



Internal ID20693748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162439557..162440102hg38UCSC Ensembl
chr5:161866563..161867108hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6413996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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