A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065605



Internal ID19154824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86256867..86677986hg38UCSC Ensembl
Innerchr16:86290473..86711592hg19UCSC Ensembl
Innerchr16:84847974..85269093hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38421120
hg19421120
hg18421120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559973
Samples
Known GenesFENDRR, FLJ30679, FOXC2, FOXF1, FOXL1, LINC00917, LINC01081, LOC146513, MTHFSD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065605
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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