A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14308385



Internal ID22126529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155133640..155133750hg38UCSC Ensembl
chr3:154851429..154851539hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204570
Supporting Variants
SamplesHG00512
Known GenesMME
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14308385
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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