A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051786



Internal ID18794317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96213058..96244781hg38UCSC Ensembl
Innerchr14:96679395..96711118hg19UCSC Ensembl
Innerchr14:95749148..95780871hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3831724
hg1931724
hg1831724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532626
Samples
Known GenesBDKRB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051786
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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