A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505032



Internal ID20878298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22088595..22568521hg38UCSC Ensembl
chr17:21666609..22067848hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38479927
hg19401240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3059n223
Supporting Variantsnssv18183350
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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