A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055774



Internal ID19144993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24184956..24413936hg38UCSC Ensembl
Innerchr19:24367758..24596738hg19UCSC Ensembl
Innerchr19:24159598..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38228981
hg19228981
hg18228981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3483n100
Supporting Variantsnssv3570666, nssv3570663, nssv3570667, nssv3570668, nssv3570670, nssv3570669, nssv3570664, nssv3570665, nssv3570662
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)nsv1055774
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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