A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225333



Internal ID22368495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155812901..155816200hg38UCSC Ensembl
chr7:155605595..155608894hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338773, nssv14338772, nssv14338776, nssv14338769, nssv14338770, nssv14338775, nssv14338774, nssv14338771, nssv14338768
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)nsv3225333
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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