A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831202



Internal ID22606137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1239628..1280651hg38UCSC Ensembl
chr2:1243400..1284423hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3841024
hg1941024
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485871
Samples
Known GenesSNTG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831202
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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