A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099532



Internal ID20666572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186668731..186706833hg38UCSC Ensembl
chr3:186386520..186424622hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3838103
hg1938103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371590
Supporting Variants
Samples
Known GenesHRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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