A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335633



Internal ID22259637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99212701..99223950hg38UCSC Ensembl
chr7:98810324..98821573hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3811250
hg1911250
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199477
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335633
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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