A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14333864



Internal ID22138724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27380056..27380221hg38UCSC Ensembl
chr7:27419675..27419840hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197948
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14333864
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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