A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202661



Internal ID22351790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42493565..42495479hg38UCSC Ensembl
chr9:44475640..44477554hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381915
hg191915
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346013, nssv14346011, nssv14346012, nssv14346010, nssv14346015, nssv14346016, nssv14346014, nssv14346017, nssv14346009
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)nsv3202661
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer