A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710772



Internal ID18662367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134280623..134340956hg38UCSC Ensembl
Innerchr11:134150517..134210850hg19UCSC Ensembl
Innerchr11:133655727..133716060hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3860334
hg1960334
hg1860334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042202
Supporting Variants
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)nssv3710772
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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