A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002114



Internal ID21911457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81436117..81436243hg38UCSC Ensembl
chr7:81065433..81065559hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002114
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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