A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335251



Internal ID22210027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85314269..85316323hg38UCSC Ensembl
chr7:84943585..84945639hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192216
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335251
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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