A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819505



Internal ID6083816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:61112694..61113306hg19UCSC Ensembl
Innerchr14:60182447..60183059hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1419027
SamplesAK1
Known GenesSIX1
Method
Analysis
PlatformIllumina CNV610 Beadchip + Illumina GA and GAII Sequencing + Illumina CNV370 Beadchip + Agilent Custom 24M CGH Array
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv819505
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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