A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844176



Internal ID22619111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163497702..163523030hg38UCSC Ensembl
chr6:163918734..163944062hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3825329
hg1925329
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502247
Samples
Known GenesQKI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844176
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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