A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046921



Internal ID19136140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81703904..81796857hg38UCSC Ensembl
Innerchr15:81996245..82089198hg19UCSC Ensembl
Innerchr15:79783300..79876253hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3892954
hg1992954
hg1892954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2635n100
Supporting Variantsnssv3554607, nssv3554605, nssv3554610, nssv3718099, nssv3554603, nssv3554606, nssv3718100, nssv3554608, nssv3554609, nssv3554604
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)nsv1046921
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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