A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528811



Internal ID20902172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62420901..62425200hg38UCSC Ensembl
chr17:60498262..60502561hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188818
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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