A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041148



Internal ID19130367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9906433..9932990hg38UCSC Ensembl
Innerchr11:9927980..9954537hg19UCSC Ensembl
Innerchr11:9884556..9911113hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826558
hg1926558
hg1826558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708515
Samples
Known GenesSBF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041148
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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