A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359389



Internal ID22127542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32500704..32539741hg38UCSC Ensembl
chr1:32966305..33005342hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3839038
hg1939038
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526538
Supporting Variants
SamplesHG00512
Known GenesZBTB8A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359389
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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