A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038512



Internal ID19127731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53511573..53559482hg38UCSC Ensembl
Innerchr15:53803770..53851679hg19UCSC Ensembl
Innerchr15:51591062..51638971hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3847910
hg1947910
hg1847910
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552426
Samples
Known GenesWDR72
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038512
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