A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517287



Internal ID20890648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2918101..2950575hg38UCSC Ensembl
chr20:2898747..2931221hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832475
hg1932475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067202
Samples
Known GenesPTPRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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