A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834905



Internal ID22609840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130915240..130927532hg38UCSC Ensembl
chr3:130634084..130646376hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3812293
hg1912293
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485042
Samples
Known GenesATP2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834905
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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