A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14308383



Internal ID22208459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155125277..155125341hg38UCSC Ensembl
chr3:154843066..154843130hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525091
Supporting Variants
SamplesHG00732
Known GenesMME
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14308383
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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