A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564842



Internal ID16005565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:51803013..51867871hg38UCSC Ensembl
Innerchr14:52269731..52334589hg19UCSC Ensembl
Innerchr14:51339481..51404339hg18UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3864859
hg1964859
hg1864859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148627
Samples1780862304_A
Known GenesGNG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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