A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511735



Internal ID20885065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27655421..27760746hg38UCSC Ensembl
chr17:25982447..26087772hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38105326
hg19105326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3065n223
Supporting Variantsnssv18034522
Samples
Known GenesNOS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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