A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335596



Internal ID22142612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98751851..98755150hg38UCSC Ensembl
chr7:98381163..98384483hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg383300
hg193321
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207603
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335596
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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