A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844292



Internal ID22619227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134903084..134931268hg38UCSC Ensembl
chr6:135224222..135252406hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3828185
hg1928185
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501607
Samples
Known GenesALDH8A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844292
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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