A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323681



Internal ID20856801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20080591..20084194hg38UCSC Ensembl
chr1:20407084..20410687hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383604
hg193604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv111n223
Supporting Variantsnssv18056918
Samples
Known GenesPLA2G5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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