A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049018



Internal ID19138237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20373039..20402808hg38UCSC Ensembl
Innerchr15:20578292..20608061hg19UCSC Ensembl
Innerchr15:18838306..18868075hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3829770
hg1929770
hg1829770
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2264n100
Supporting Variantsnssv3535843, nssv3535844, nssv3713815
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)nsv1049018
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer