A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048701



Internal ID19137920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:35628310..35652772hg38UCSC Ensembl
Innerchr11:35649858..35674320hg19UCSC Ensembl
Innerchr11:35606434..35630896hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3824463
hg1924463
hg1824463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518376
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)nsv1048701
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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