A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013106



Internal ID21922449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107003635..107003754hg38UCSC Ensembl
chr7:106644080..106644199hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013106
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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