A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319051



Internal ID20852143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110629895..110633343hg38UCSC Ensembl
chr1:111172517..111175965hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg383449
hg193449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050857
Samples
Known GenesKCNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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