A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035263



Internal ID20602303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38304750..38316959hg38UCSC Ensembl
chr17:36460716..36472859hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812210
hg1912144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503966
Supporting Variants
Samples
Known GenesMRPL45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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