A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747606



Internal ID20523625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10550740..10557138hg38UCSC Ensembl
chr19:10661416..10667814hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386399
hg196399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274542
Samples
Known GenesATG4D, KRI1, MIR1238
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747606
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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