A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049031



Internal ID19138250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38930902..39199711hg38UCSC Ensembl
Innerchr11:38952452..39221261hg19UCSC Ensembl
Innerchr11:38909028..39177837hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38268810
hg19268810
hg18268810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519832
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)nsv1049031
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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