A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508693



Internal ID20881997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44569997..44578278hg38UCSC Ensembl
chr15:44862195..44870476hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg388282
hg198282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024568
Samples
Known GenesSPG11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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