A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515349



Internal ID20888708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39930278..39941368hg38UCSC Ensembl
chr17:38086531..38097621hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811091
hg1911091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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