A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844063



Internal ID22618998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144766224..144770669hg38UCSC Ensembl
chr6:145087360..145091805hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384446
hg194446
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501838
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844063
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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