A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201530



Internal ID22350823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101614351..101636100hg38UCSC Ensembl
chr7:101257631..101279380hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3821750
hg1921750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336412, nssv14336417, nssv14336413, nssv14336414, nssv14336418, nssv14336415, nssv14336416, nssv14336420, nssv14336419
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesMYL10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201530
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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