A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551512



Internal ID15992235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72012256..72031061hg38UCSC Ensembl
Innerchr10:73772014..73790819hg19UCSC Ensembl
Innerchr10:73442020..73460825hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3818806
hg1918806
hg1818806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750269
Samples
Known GenesCHST3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551512
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