A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332891



Internal ID20866066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23917618..23930273hg38UCSC Ensembl
chr1:24244108..24256763hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812656
hg1912656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202521
Samples
Known GenesMIR378F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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