A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452915



Internal ID21110468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119635809..119638563hg38UCSC Ensembl
chr10:121395321..121398075hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382755
hg192755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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