A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143237



Internal ID20710277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17110607..17112574hg38UCSC Ensembl
chr6:17110838..17112805hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381968
hg191968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402973
Supporting Variants
Samples
Known GenesSTMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00082


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