A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443839



Internal ID21101392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86090801..86092100hg38UCSC Ensembl
chr10:87850558..87851857hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984464
Samples
Known GenesGRID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443839
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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