A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188186



Internal ID20755226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15555401..15575900hg38UCSC Ensembl
chr17:15458715..15479214hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820500
hg1920500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501981
Supporting Variants
Samples
Known GenesCDRT1, TVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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