A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001461



Internal ID21910804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146035594..146045965hg38UCSC Ensembl
chr7:145732687..145743058hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3810372
hg1910372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001461
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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