A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336168



Internal ID20993721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160041209..160043181hg38UCSC Ensembl
chr2:160897720..160899692hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381973
hg191973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080517
Samples
Known GenesPLA2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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