A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17568143



Internal ID21760186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100991701..100991701hg38UCSC Ensembl
chr7:100634982..100634982hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073022
Supporting Variants
Samples
Known GenesMUC12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17568143
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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