A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548077



Internal ID21872432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41717400..41717400hg38UCSC Ensembl
chr4:41719417..41719417hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548077
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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