A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204661



Internal ID21343463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102541898..102541898hg38UCSC Ensembl
chr8:103554126..103554126hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382327
hg192327
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944824
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204661
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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