A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052666



Internal ID19141885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81602818..82562038hg38UCSC Ensembl
Innerchr14:82069162..83028382hg19UCSC Ensembl
Innerchr14:81138915..82098135hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38959221
hg19959221
hg18959221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531227
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)nsv1052666
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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