A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448349



Internal ID21105902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19847322..19860065hg38UCSC Ensembl
chr10:20136251..20148994hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3812744
hg1912744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979049
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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