A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018138



Internal ID21927481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121172697..121261729hg38UCSC Ensembl
chr7:120812751..120901783hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3889033
hg1989033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570968
Samples
Known GenesCPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018138
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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