A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556150



Internal ID15996873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102464878..102545128hg38UCSC Ensembl
Innerchr11:102335609..102415859hg19UCSC Ensembl
Innerchr11:101840819..101921069hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3880251
hg1980251
hg1880251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2136n54
Supporting Variantsnssv1174949
SamplesHGDP00570
Known GenesMMP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556150
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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