A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552548



Internal ID20925674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42505154..42519233hg38UCSC Ensembl
chr20:41133794..41147873hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3814080
hg1914080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067494
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552548
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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