A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035985



Internal ID19125204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94421340..94442795hg38UCSC Ensembl
Innerchr14:94887677..94909132hg19UCSC Ensembl
Innerchr14:93957430..93978885hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3821456
hg1921456
hg1821456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1963n100
Supporting Variantsnssv3532620
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)nsv1035985
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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