A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829096



Internal ID22604031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205374042..205379957hg38UCSC Ensembl
chr1:205343170..205349085hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg385916
hg195916
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451684
Samples
Known GenesLEMD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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