A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748802



Internal ID20524829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34372011..34373018hg38UCSC Ensembl
chr6:34339788..34340795hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280844
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748802
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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