A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181674



Internal ID20748714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43537515..43634172hg38UCSC Ensembl
chr17:41614883..41711540hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3896658
hg1996658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504040
Supporting Variants
Samples
Known GenesETV4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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