A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449995



Internal ID21107548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33914130..33920854hg38UCSC Ensembl
chr10:34203058..34209782hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg386725
hg196725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449995
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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