A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557562



Internal ID21881917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93888584..93888584hg38UCSC Ensembl
chr7:93517896..93517896hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070313
Supporting Variants
Samples
Known GenesTFPI2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557562
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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