A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169916



Internal ID21313727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51931733..51939345hg38UCSC Ensembl
Outerchr10:51930530..51947799hg38UCSC Ensembl
Innerchr10:53691493..53699105hg19UCSC Ensembl
Outerchr10:53690290..53707559hg19UCSC Ensembl
Innerchr10:53361499..53369111hg18UCSC Ensembl
Outerchr10:53360296..53377565hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3817270
hg1917270
hg1817270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242155
SamplesMLY_14
Known GenesPRKG1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169916
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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