A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885360



Internal ID22660344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60976565..61000114hg38UCSC Ensembl
chr2:61203700..61227249hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3823550
hg1923550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407867
Samples
Known GenesPUS10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885360
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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