A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833152



Internal ID22608087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:261648..267447hg38UCSC Ensembl
chr2:261648..267447hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484070
Samples
Known GenesACP1, SH3YL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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