A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050374



Internal ID19139593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53382529..53493070hg38UCSC Ensembl
Innerchr15:53674726..53785267hg19UCSC Ensembl
Innerchr15:51462018..51572559hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38110542
hg19110542
hg18110542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2600n100
Supporting Variantsnssv3716730
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050374
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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