A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565987



Internal ID16353396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103519818..103522370hg38UCSC Ensembl
Innerchr14:103986155..103988707hg19UCSC Ensembl
Innerchr14:103055908..103058460hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382553
hg192553
hg182553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3938n54
Supporting Variantsnssv834337
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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