A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496308



Internal ID20869508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101069973..101078149hg38UCSC Ensembl
chr15:101610178..101618354hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388177
hg198177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022954
Samples
Known GenesLRRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496308
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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