A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844620



Internal ID22619555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139864365..139865364hg38UCSC Ensembl
chr6:140185502..140186501hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501784, nssv17501783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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