A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201438



Internal ID22350746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392627..66395111hg38UCSC Ensembl
chr7:65857614..65860098hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382485
hg192485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8566n152
Supporting Variantsnssv14335752, nssv14335750, nssv14335754, nssv14335755, nssv14335751, nssv14335753, nssv14335749
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00513, HG00514
Known GenesLINC00174
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201438
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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