A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336836



Internal ID22198474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105553426..105553695hg38UCSC Ensembl
chr7:105193873..105194142hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527095
Supporting Variants
SamplesHG00732
Known GenesRINT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336836
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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