A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199669



Internal ID21338465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140595787..140595844hg38UCSC Ensembl
chr8:141605886..141605943hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935409
Supporting Variants
SamplesHG002
Known GenesAGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199669
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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