A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098475



Internal ID20665515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183137101..183138800hg38UCSC Ensembl
chr3:182854889..182856588hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372725
Supporting Variants
Samples
Known GenesLAMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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