A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039172



Internal ID20606212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9881368..9881675hg38UCSC Ensembl
chr17:9784685..9784992hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502651
Supporting Variants
Samples
Known GenesGLP2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.05146


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer