A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530138



Internal ID18828419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40049637..40147703hg38UCSC Ensembl
Innerchr14:40518841..40616907hg19UCSC Ensembl
Innerchr14:39588592..39686658hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3898067
hg1998067
hg1898067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051963
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)nssv3530138
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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