A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564042



Internal ID16351451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23399076..23406784hg38UCSC Ensembl
Innerchr14:23868285..23875993hg19UCSC Ensembl
Innerchr14:22938125..22945833hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg387709
hg197709
hg187709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824366
Samples
Known GenesMYH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564042
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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