A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv770706



Internal ID16064662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31372513..31375263hg38UCSC Ensembl
Innerchr11:31394060..31396810hg19UCSC Ensembl
Innerchr11:31350636..31353386hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382751
hg192751
hg182751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553959
Supporting Variants
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv770706
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