A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324087



Internal ID20857211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19899776..19903144hg38UCSC Ensembl
chr1:20226269..20229637hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg383369
hg193369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056856
Samples
Known GenesOTUD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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