A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515311



Internal ID20888670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20900729..20990969hg38UCSC Ensembl
chr17:20804042..20894282hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3890241
hg1990241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185922
Samples
Known GenesLOC440416
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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