A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443958



Internal ID21101511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91973206..91975496hg38UCSC Ensembl
chr10:93732963..93735253hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg382291
hg192291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985384
Samples
Known GenesBTAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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