A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551117



Internal ID16338526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57178792..57247982hg38UCSC Ensembl
Innerchr10:58938552..59007742hg19UCSC Ensembl
Innerchr10:58608558..58677748hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3869191
hg1969191
hg1869191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv748619
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551117
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