A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034475



Internal ID20601515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2429434..2430060hg38UCSC Ensembl
chr17:2332728..2333354hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514342
Supporting Variants
Samples
Known GenesMETTL16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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