A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122100



Internal ID20689140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102548302..102548952hg38UCSC Ensembl
chr5:101884006..101884656hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411194
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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