A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843644



Internal ID22618579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10811816..10814235hg38UCSC Ensembl
chr6:10812049..10814468hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg382420
hg192420
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500892
Samples
Known GenesMAK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843644
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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