A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051847



Internal ID19141066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94422318..94445260hg38UCSC Ensembl
Innerchr14:94888655..94911597hg19UCSC Ensembl
Innerchr14:93958408..93981350hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3822943
hg1922943
hg1822943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1963n100
Supporting Variantsnssv3711384
Samples
Known GenesSERPINA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051847
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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