A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14365010



Internal ID22145319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95286010..95286796hg38UCSC Ensembl
chr12:95679786..95680572hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38787
hg19787
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211738
Supporting Variants
SamplesHG00514
Known GenesVEZT
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14365010
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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