A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442052



Internal ID21099605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107446301..107490600hg38UCSC Ensembl
chr10:109206059..109250358hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3844300
hg1944300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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