A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036590



Internal ID20603630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4772769..4787562hg38UCSC Ensembl
chr17:4676064..4690857hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3814794
hg1914794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505175
Supporting Variants
Samples
Known GenesTM4SF5, VMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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