A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033902



Internal ID20600942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15515901..15593300hg38UCSC Ensembl
chr17:15419215..15496614hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3877400
hg1977400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500152
Supporting Variants
Samples
Known GenesCDRT1, TVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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