A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844648



Internal ID22619583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149668160..149673419hg38UCSC Ensembl
chr6:149989296..149994555hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385260
hg195260
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502409
Samples
Known GenesLATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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