A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035257



Internal ID18777788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134282136..134347316hg38UCSC Ensembl
Innerchr11:134152030..134217210hg19UCSC Ensembl
Innerchr11:133657240..133722420hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3865181
hg1965181
hg1865181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1302n100
Supporting Variantsnssv3503592
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)nsv1035257
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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