A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844149



Internal ID22619084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158579107..158580106hg38UCSC Ensembl
chr6:159000139..159001138hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502499
Samples
Known GenesTMEM181
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844149
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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