A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036793



Internal ID18779324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78198402..78265821hg38UCSC Ensembl
Innerchr11:77909448..77976867hg19UCSC Ensembl
Innerchr11:77587096..77654515hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3867420
hg1967420
hg1867420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505483
Samples
Known GenesGAB2, USP35
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036793
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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