A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184946



Internal ID20751986
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 StatusS
Merged Variantsnsv6442915
Supporting Variants
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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