A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198822



Internal ID21337618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69452001..69452089hg38UCSC Ensembl
chr8:70364236..70364324hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951997
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198822
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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