A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831235



Internal ID22606170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12994060..13001451hg38UCSC Ensembl
chr2:13134185..13141576hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg387392
hg197392
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486365
Samples
Known GenesLOC100506474
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831235
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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