A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100460



Internal ID20667500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18036094..18036824hg38UCSC Ensembl
chr3:18077586..18078316hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369652
Supporting Variants
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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