A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336414



Internal ID22183524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101614351..101636100hg38UCSC Ensembl
chr7:101257631..101279380hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3821750
hg1921750
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201530
Supporting Variants
SamplesHG00514
Known GenesMYL10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336414
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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