A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368812



Internal ID21026365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77315128..77318806hg38UCSC Ensembl
chr3:77364279..77367957hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383679
hg193679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105163
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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