A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325046



Internal ID20858176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24179001..24201900hg38UCSC Ensembl
chr1:24505491..24528390hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3822900
hg1922900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200616
Samples
Known GenesIFNLR1, LOC284632
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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