A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840772



Internal ID22615707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126583962..126595546hg38UCSC Ensembl
chr5:125919654..125931238hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3811585
hg1911585
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494170
Samples
Known GenesALDH7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840772
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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