A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454718



Internal ID21112271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102148863..102152999hg38UCSC Ensembl
chr10:103908620..103912756hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg384137
hg194137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193543
Samples
Known GenesNOLC1, PPRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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