A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452397



Internal ID21109950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15136000..15141177hg38UCSC Ensembl
chr10:15177999..15183176hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385178
hg195178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179131
Samples
Known GenesNMT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452397
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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