A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860536



Internal ID22635471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98493342..98495775hg38UCSC Ensembl
chr12:98887120..98889553hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382434
hg192434
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449877
Samples
Known GenesLOC643770
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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