A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335716



Internal ID22323252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66025364..66025791hg38UCSC Ensembl
chr7:65490351..65490778hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528566
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335716
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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