A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505761



Internal ID20879034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30377901..30391300hg38UCSC Ensembl
chr17:28704919..28718318hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196172
Samples
Known GenesCPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505761
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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