A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542684



Internal ID21867039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108028454..108028454hg38UCSC Ensembl
chr4:108949610..108949610hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067810
Supporting Variants
Samples
Known GenesHADH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542684
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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