A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035715



Internal ID20602755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43589962..43590964hg38UCSC Ensembl
chr17:41667330..41668332hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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