A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100497



Internal ID20667537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186210614..186214031hg38UCSC Ensembl
chr3:185928403..185931820hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383418
hg193418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367825
Supporting Variants
Samples
Known GenesDGKG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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