A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534491



Internal ID20907852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57574415..57579471hg38UCSC Ensembl
chr17:55651776..55656832hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg385057
hg195057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188608
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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