A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184699



Internal ID20751739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49338230..49343125hg38UCSC Ensembl
chr17:47415592..47420487hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg384896
hg194896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516676
Supporting Variants
Samples
Known GenesZNF652
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184699
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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