A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524738



Internal ID20898099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58896415..58897300hg38UCSC Ensembl
chr17:56973776..56974661hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38886
hg19886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186558
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524738
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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