A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039271



Internal ID19128490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83939217..84001206hg38UCSC Ensembl
Innerchr14:84405561..84467550hg19UCSC Ensembl
Innerchr14:83475314..83537303hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3861990
hg1961990
hg1861990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532360
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039271
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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