A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332246



Internal ID20865416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21551759..21555804hg38UCSC Ensembl
chr1:21878252..21882297hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg384046
hg194046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200567
Samples
Known GenesALPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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