A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444368



Internal ID21101921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101432143..101672706hg38UCSC Ensembl
chr10:103191900..103432463hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38240564
hg19240564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187867
Samples
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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