A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370760



Internal ID21028313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87249438..87249812hg38UCSC Ensembl
chr3:87298588..87298962hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104175
Samples
Known GenesCHMP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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