A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132036



Internal ID20699076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37698219..37698880hg38UCSC Ensembl
chr5:37698321..37698982hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377062
Supporting Variants
Samples
Known GenesWDR70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132036
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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