A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201034



Internal ID21339840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:104312281..104312281hg38UCSC Ensembl
chr5:103647982..103647982hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940260
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201034
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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