A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331375



Internal ID20864538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210986364..211012655hg38UCSC Ensembl
chr1:211159706..211185997hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3826292
hg1926292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057394
Samples
Known GenesKCNH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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