A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531227



Internal ID18829508
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 StatusS
Merged Variantsnsv1052666
Supporting Variants
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)nssv3531227
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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