A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047161



Internal ID19136380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87353751..87370306hg38UCSC Ensembl
Innerchr15:87896982..87913537hg19UCSC Ensembl
Innerchr15:85697986..85714541hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3816556
hg1916556
hg1816556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2656n100
Supporting Variantsnssv3555188
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)nsv1047161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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