A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505539



Internal ID20878810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15730801..15763500hg38UCSC Ensembl
chr17:15634115..15666814hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3832700
hg1932700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3008n223
Supporting Variantsnssv18196102
Samples
Known GenesTBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505539
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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