A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035295



Internal ID18777826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:80714655..80770292hg38UCSC Ensembl
Innerchr14:81180999..81236636hg19UCSC Ensembl
Innerchr14:80250752..80306389hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3855638
hg1955638
hg1855638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531225
Samples
Known GenesCEP128
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035295
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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