A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527095



Internal ID22396479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105553426..105553695hg38UCSC Ensembl
chr7:105193873..105194142hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336832, nssv14336840, nssv14336839, nssv14336838, nssv14336834, nssv14336835, nssv14336833, nssv14336837, nssv14336836
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesRINT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527095
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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