A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5827958



Internal ID22602893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12703593..12725481hg38UCSC Ensembl
chr1:12763595..12785448hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3821889
hg1921854
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462356
Samples
Known GenesAADACL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5827958
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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