A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204904



Internal ID21343707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63440213..63440213hg38UCSC Ensembl
chr8:64352771..64352771hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946987
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204904
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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