A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564265



Internal ID16004988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35043129..35155625hg38UCSC Ensembl
Innerchr14:35512335..35624831hg19UCSC Ensembl
Innerchr14:34582086..34694582hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38112497
hg19112497
hg18112497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825349, nssv825347, nssv825350, nssv825348
Samples
Known GenesFAM177A1, KIAA0391, PPP2R3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564265
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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