A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412295



Internal ID21069848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34347115..34364638hg38UCSC Ensembl
chr6:34314892..34332415hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3817524
hg1917524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140882
Samples
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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