A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520665



Internal ID20894026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64143755..64149673hg38UCSC Ensembl
chr17:62221115..62227033hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg385919
hg195919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186003
Samples
Known GenesSNORA76, SNORD104, TEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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