A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187911



Internal ID20754951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35996686..36006924hg38UCSC Ensembl
chr17:34323722..34333967hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810239
hg1910246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506241
Supporting Variants
Samples
Known GenesCCL15, CCL15-CCL14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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