A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844647



Internal ID22619582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149626573..149628376hg38UCSC Ensembl
chr6:149947709..149949512hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381804
hg191804
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501650
Samples
Known GenesKATNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844647
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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