A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521999



Internal ID20895360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63269018..63453355hg38UCSC Ensembl
chr17:61346379..61530716hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38184338
hg19184338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193115
Samples
Known GenesCYB561, TANC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521999
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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