A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844046



Internal ID22618981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138885204..138886803hg38UCSC Ensembl
chr6:139206341..139207940hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501772
Samples
Known GenesECT2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844046
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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