A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062651



Internal ID19151870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27525373hg38UCSC Ensembl
Innerchr19:27747981..28016281hg19UCSC Ensembl
Innerchr19:32439821..32708121hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38268301
hg19268301
hg18268301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3497n100
Supporting Variantsnssv3571971, nssv3571972, nssv3570863, nssv3570862, nssv3570861, nssv3571973
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)nsv1062651
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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