A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228376



Internal ID22370581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156154251..156160250hg38UCSC Ensembl
chr7:155946945..155952944hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338833, nssv14338828, nssv14338831, nssv14338834, nssv14338830, nssv14338836, nssv14338829, nssv14338832, nssv14338835
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228376
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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