A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14333482



Internal ID22147377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43834867..43834936hg38UCSC Ensembl
chr7:43874466..43874535hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529246
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14333482
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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