A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199655



Internal ID21338451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139463015..139463347hg38UCSC Ensembl
chr8:140475258..140475590hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942823
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199655
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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