A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035784



Internal ID18778315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77069929..77177597hg38UCSC Ensembl
Innerchr11:76780975..76888643hg19UCSC Ensembl
Innerchr11:76458623..76566291hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38107669
hg19107669
hg18107669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1230n100
Supporting Variantsnssv3519651, nssv3508475, nssv3513244, nssv3513509, nssv3521463
Samples
Known GenesCAPN5, MYO7A, OMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035784
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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