A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517269



Internal ID20890630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57930834..57940394hg38UCSC Ensembl
chr17:56008195..56017755hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg389561
hg199561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196864
Samples
Known GenesCUEDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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