A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843761



Internal ID22618696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134305392..134307591hg38UCSC Ensembl
chr6:134626530..134628729hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501605
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843761
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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