A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198910



Internal ID21337706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143015612..143015719hg38UCSC Ensembl
chr8:144097029..144097136hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934962
Supporting Variants
SamplesHG002
Known GenesLOC100133669
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198910
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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