A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570968



Internal ID21763011
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 StatusS
Merged Variantsnsv6018138
Supporting Variants
Samples
Known GenesCPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570968
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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