A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194497



Internal ID20761537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14018701..14025000hg38UCSC Ensembl
chr17:13922018..13928317hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496521
Supporting Variants
Samples
Known GenesCDRT15P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194497
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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