A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543756



Internal ID21868111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38734174..38734174hg38UCSC Ensembl
chr4:38735795..38735795hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543756
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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