A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557333



Internal ID21881688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144725583..144725583hg38UCSC Ensembl
chr4:145646735..145646735hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080141
Supporting Variants
Samples
Known GenesHHIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557333
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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