A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834978



Internal ID22609913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148058633..148061934hg38UCSC Ensembl
chr3:147776420..147779721hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834978
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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