A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050145



Internal ID19139364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37319835..37360412hg38UCSC Ensembl
Innerchr11:37341385..37381962hg19UCSC Ensembl
Innerchr11:37297961..37338538hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3840578
hg1940578
hg1840578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n100
Supporting Variantsnssv3519437
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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