A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753228



Internal ID16047184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89159378..89204269hg38UCSC Ensembl
Innerchr10:90919135..90964026hg19UCSC Ensembl
Innerchr10:90909115..90954006hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3844892
hg1944892
hg1844892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551845
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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