A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051670



Internal ID19140889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20418941hg38UCSC Ensembl
Innerchr15:20585976..20624194hg19UCSC Ensembl
Innerchr15:18845990..18884208hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3838219
hg1938219
hg1838219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2275n100
Supporting Variantsnssv3537140, nssv3537141, nssv3537145, nssv3537144, nssv3537142, nssv3537143
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)nsv1051670
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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