A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582194



Internal ID21774237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94261915..94261915hg38UCSC Ensembl
chr8:95274143..95274143hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067060
Supporting Variants
Samples
Known GenesGEM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582194
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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