A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5546997



Internal ID320889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10685912..10685912hg38UCSC Ensembl
chr2:10826038..10826038hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909441
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5546997
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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