A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036156



Internal ID20603196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50082397..50088881hg38UCSC Ensembl
chr17:48159761..48166245hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg386485
hg196485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526697
Supporting Variants
Samples
Known GenesITGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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