A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051769



Internal ID18794300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119702155..119760060hg38UCSC Ensembl
Innerchr11:119572865..119630769hg19UCSC Ensembl
Innerchr11:119078075..119135979hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3857906
hg1957905
hg1857905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521726
Samples
Known GenesPVRL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051769
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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