A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200954



Internal ID21339755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2145621..2145621hg38UCSC Ensembl
chr5:2145735..2145735hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937118
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200954
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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