A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050949



Internal ID19140168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35265824..35477611hg38UCSC Ensembl
Innerchr15:35558025..35769812hg19UCSC Ensembl
Innerchr15:33345317..33557104hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38211788
hg19211788
hg18211788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716698
Samples
Known GenesDPH6, MIR3942
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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