A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742748



Internal ID20518733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14894352..14894670hg38UCSC Ensembl
chr10:14936351..14936669hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261004
Samples
Known GenesSUV39H2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742748
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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