A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317337



Internal ID20850421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24167418..24196841hg38UCSC Ensembl
chr1:24493908..24523331hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3829424
hg1929424
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200614
Samples
Known GenesIFNLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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