A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105064



Internal ID20672104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99832287..99925668hg38UCSC Ensembl
chr3:99551131..99644512hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3893382
hg1993382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369842
Supporting Variants
Samples
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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