A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332841



Internal ID20866016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21648701..21652000hg38UCSC Ensembl
chr1:21975194..21978493hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057517
Samples
Known GenesRAP1GAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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