A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204162



Internal ID21342964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142970296..142970296hg38UCSC Ensembl
chr8:144051713..144051713hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936412
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204162
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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