A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447851



Internal ID21105404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49677501..49681800hg38UCSC Ensembl
chr10:50885547..50889846hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196910
Samples
Known GenesC10orf53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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