A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529681



Internal ID22399072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125076611..125076994hg38UCSC Ensembl
chr9:127838890..127839273hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347701, nssv14347694, nssv14347697, nssv14347699, nssv14347698, nssv14347700, nssv14347695, nssv14347693, nssv14347696
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesSCAI
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529681
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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