A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035700



Internal ID19124919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113610250..113671276hg38UCSC Ensembl
Innerchr11:113480972..113541998hg19UCSC Ensembl
Innerchr11:112986182..113047208hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3861027
hg1961027
hg1861027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504062
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)nsv1035700
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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