A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017592



Internal ID21926935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66098086..66099872hg38UCSC Ensembl
chr7:65563073..65564859hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381787
hg191787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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