A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513167



Internal ID20886508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28764403..28766418hg38UCSC Ensembl
chr17:27091421..27093436hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382016
hg192016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179711
Samples
Known GenesFAM222B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513167
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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