A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034269



Internal ID20601309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20818997..20820945hg38UCSC Ensembl
chr17:20722310..20724258hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381949
hg191949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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