A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv781668



Internal ID16075624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97384512..97555631hg38UCSC Ensembl
Innerchr11:97255512..97426631hg19UCSC Ensembl
Innerchr11:96760722..96931841hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38171120
hg19171120
hg18171120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555993
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv781668
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