A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565510



Internal ID16006233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87928587..87961245hg38UCSC Ensembl
Innerchr14:88394931..88427589hg19UCSC Ensembl
Innerchr14:87464684..87497342hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3832659
hg1932659
hg1832659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3840n54
Supporting Variantsnssv832170
Samples
Known GenesGALC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565510
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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