A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012252



Internal ID21921595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170150057..170150137hg38UCSC Ensembl
chr5:169577061..169577141hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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