A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442915



Internal ID21100468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19861105..19870496hg38UCSC Ensembl
chr10:20150034..20159425hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389392
hg199392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184946
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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