A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551774



Internal ID16339183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86341610..86368524hg38UCSC Ensembl
Innerchr10:88101367..88128281hg19UCSC Ensembl
Innerchr10:88091347..88118261hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3826915
hg1926915
hg1826915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752214
Samples
Known GenesGRID1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551774
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