A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447599



Internal ID21105152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6205605..6210622hg38UCSC Ensembl
chr10:6247568..6252585hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385018
hg195018
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182356
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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