A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764490



Internal ID16058446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2158083..2162736hg38UCSC Ensembl
Innerchr11:2179313..2183966hg19UCSC Ensembl
Innerchr11:2135889..2140542hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384654
hg194654
hg184654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553077
Supporting Variants
Samples
Known GenesINS, INS-IGF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764490
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