A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553908



Internal ID16341317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26640143..26652486hg38UCSC Ensembl
Innerchr11:26661690..26674033hg19UCSC Ensembl
Innerchr11:26618266..26630609hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg3812344
hg1912344
hg1812344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174782
Samples1780854538_A
Known GenesANO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553908
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