A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193547



Internal ID20760587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11761072..11811700hg38UCSC Ensembl
chr17:11664389..11715017hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3850629
hg1950629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497259
Supporting Variants
Samples
Known GenesDNAH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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