A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339970



Internal ID20997523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51301..1526300hg38UCSC Ensembl
chr3:92984..1567984hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381475000
hg191475001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4741n223
Supporting Variantsnssv18102884
Samples
Known GenesCHL1, CNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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