A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565507



Internal ID16006230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87928587..87953014hg38UCSC Ensembl
Innerchr14:88394931..88419358hg19UCSC Ensembl
Innerchr14:87464684..87489111hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3824428
hg1924428
hg1824428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3840n54
Supporting Variantsnssv832165
Samples
Known GenesGALC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565507
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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