A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020325



Internal ID21929668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20121843..20121907hg38UCSC Ensembl
chr7:20161466..20161530hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020325
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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