A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843984



Internal ID22618919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10800353..10812762hg38UCSC Ensembl
chr6:10800586..10812995hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3812410
hg1912410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501056
Samples
Known GenesMAK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843984
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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