A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744008



Internal ID20520002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18441977..18443324hg38UCSC Ensembl
chr19:18552787..18554134hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381348
hg191348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284993
Samples
Known GenesELL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744008
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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