A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036841



Internal ID19126060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84917875..84950132hg38UCSC Ensembl
Innerchr15:85461106..85493363hg19UCSC Ensembl
Innerchr15:83262110..83294367hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3832258
hg1932258
hg1832258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2646n100
Supporting Variantsnssv3555057, nssv3555056, nssv3718139
Samples
Known GenesSLC28A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036841
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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