A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047584



Internal ID19136803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20364686..20512131hg38UCSC Ensembl
Innerchr15:20569939..20717374hg19UCSC Ensembl
Innerchr15:18829953..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38147446
hg19147436
hg18147436
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2243n100
Supporting Variantsnssv3713798, nssv3537647, nssv3713799, nssv3537648
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)nsv1047584
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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