A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451629



Internal ID21109182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97031801..97113931hg38UCSC Ensembl
chr10:98791558..98873688hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3882131
hg1982131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179944
Samples
Known GenesLOC100505540, SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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