A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332773



Internal ID22200454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39914087..39914600hg38UCSC Ensembl
chr7:39953686..39954199hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200123
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332773
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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