A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036028



Internal ID19125247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33140899..33202974hg38UCSC Ensembl
Innerchr14:33610105..33672180hg19UCSC Ensembl
Innerchr14:32679856..32741931hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3862076
hg1962076
hg1862076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712276
Samples
Known GenesNPAS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036028
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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