A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565646



Internal ID16353055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96178700..96193336hg38UCSC Ensembl
Innerchr14:96645037..96659673hg19UCSC Ensembl
Innerchr14:95714790..95729426hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3814637
hg1914637
hg1814637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148966
Samples1780854392_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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