A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844727



Internal ID22619662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144190127..144193197hg38UCSC Ensembl
chr6:144511264..144514334hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383071
hg193071
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501834
Samples
Known GenesSTX11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844727
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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