A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034394



Internal ID20601434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14493675..14503850hg38UCSC Ensembl
chr17:14396992..14407167hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3810176
hg1910176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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