A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335093



Internal ID22267834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81080270..81080456hg38UCSC Ensembl
chr7:80709586..80709772hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528819
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335093
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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