A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137247



Internal ID20704287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117588526..117590242hg38UCSC Ensembl
chr6:117909689..117911405hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg381717
hg191717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617320
Supporting Variants
Samples
Known GenesGOPC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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