A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204095



Internal ID21342877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73067663..73067663hg38UCSC Ensembl
chr8:73979898..73979898hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937231
Supporting Variants
SamplesHG002
Known GenesSBSPON
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204095
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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