A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053478



Internal ID19142697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20441310hg38UCSC Ensembl
Innerchr15:20581439..20646563hg19UCSC Ensembl
Innerchr15:18841453..18906577hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3865125
hg1965125
hg1865125
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2273n100
Supporting Variantsnssv3535879, nssv3535881, nssv3535880
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053478
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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