A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447405



Internal ID21104958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99398587..99399957hg38UCSC Ensembl
chr10:101158344..101159714hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg381371
hg191371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985866
Samples
Known GenesGOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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