A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056917



Internal ID20623958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20080485..20088032hg38UCSC Ensembl
chr1:20406978..20414525hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325920
Supporting Variants
Samples
Known GenesPLA2G5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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