A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833052



Internal ID22607987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55407086..55409085hg38UCSC Ensembl
chr2:55634222..55636221hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486894
Samples
Known GenesCCDC88A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833052
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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