A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515354



Internal ID20888713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2408604..2652348hg38UCSC Ensembl
chr17:2311898..2555642hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38243745
hg19243745
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2974n223
Supporting Variantsnssv18191465
Samples
Known GenesLOC284009, METTL16, PAFAH1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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