A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443225



Internal ID21100778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23438601..23441400hg38UCSC Ensembl
chr10:23727530..23730329hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979733
Samples
Known GenesOTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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