A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453636



Internal ID21111189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4827838..5181266hg38UCSC Ensembl
chr10:4870030..5223229hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38353429
hg19353200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv601n223
Supporting Variantsnssv17979975
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C6P, AKR1CL1, AKR1E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453636
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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