A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843734



Internal ID22618669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122536502..122547676hg38UCSC Ensembl
chr6:122857647..122868821hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3811175
hg1911175
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501122
Samples
Known GenesPKIB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843734
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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