A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500132



Internal ID20873357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44564283..44566954hg38UCSC Ensembl
chr15:44856481..44859152hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382672
hg192672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024566
Samples
Known GenesSPG11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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