A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361735



Internal ID21019288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46405240..46412837hg38UCSC Ensembl
chr3:46446731..46454328hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg387598
hg197598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100702
Samples
Known GenesCCRL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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