A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327642



Internal ID20860782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20068574..20075912hg38UCSC Ensembl
chr1:20395067..20402405hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387339
hg197339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056908
Samples
Known GenesPLA2G5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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