A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503504



Internal ID20876759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44593896..44672852hg38UCSC Ensembl
chr15:44886094..44965050hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3878957
hg1978957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024569
Samples
Known GenesPATL2, SPG11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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