A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844591



Internal ID22619526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2927524..2930980hg38UCSC Ensembl
chr6:2927758..2931214hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383457
hg193457
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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