A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985297



Internal ID21894640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10743861..10743921hg38UCSC Ensembl
chr2:10883987..10884047hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524532
Samples
Known GenesATP6V1C2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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