A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038713



Internal ID18781244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134282136..134340635hg38UCSC Ensembl
Innerchr11:134152030..134210529hg19UCSC Ensembl
Innerchr11:133657240..133715739hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3858500
hg1958500
hg1858500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1302n100
Supporting Variantsnssv3510365
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038713
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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