A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452516



Internal ID21110069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6290568..6293415hg38UCSC Ensembl
chr10:6332531..6335378hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192021
Samples
Known GenesLOC399715
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452516
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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