A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411506



Internal ID22469376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107654722..107654722hg38UCSC Ensembl
chr6:107975926..107975926hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956742
Supporting Variants
Samples
Known GenesSOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411506
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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