A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357767



Internal ID21015320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105823221..105823886hg38UCSC Ensembl
chr3:105542065..105542730hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093693
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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