A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052987



Internal ID19142206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76358893..76552223hg38UCSC Ensembl
Innerchr14:76825236..77018566hg19UCSC Ensembl
Innerchr14:75894989..76088319hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38193331
hg19193331
hg18193331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1942n100
Supporting Variantsnssv3713527
Samples
Known GenesESRRB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052987
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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