A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450720



Internal ID21108273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6973550..7162777hg38UCSC Ensembl
chr10:7015512..7204739hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38189228
hg19189228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182745
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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