A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039169



Internal ID20606209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9800429..9989021hg38UCSC Ensembl
chr17:9703746..9892338hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38188593
hg19188593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501670
Supporting Variants
Samples
Known GenesGAS7, GLP2R, RCVRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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