A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105159



Internal ID20672200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77298616..77304726hg38UCSC Ensembl
chr3:77347767..77353877hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359357
Supporting Variants
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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