A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844305



Internal ID22619240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11050074..11051373hg38UCSC Ensembl
chr6:11050307..11051606hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500916, nssv17500917
Samples
Known GenesELOVL2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844305
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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