A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844264



Internal ID22619199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12456668..12457681hg38UCSC Ensembl
chr6:12456900..12457913hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381014
hg191014
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844264
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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