A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843985



Internal ID22618920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108345601..108356938hg38UCSC Ensembl
chr6:108666805..108678142hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811338
hg1911338
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500897
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843985
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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