A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009583



Internal ID21918926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25258939..25258995hg38UCSC Ensembl
chr7:25298558..25298614hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009583
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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