A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332889



Internal ID22201663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:419392..420103hg38UCSC Ensembl
chr7:459358..460069hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193260
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332889
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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