A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048828



Internal ID19138047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52958686..52996597hg38UCSC Ensembl
Innerchr15:53250883..53288794hg19UCSC Ensembl
Innerchr15:51038175..51076086hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3837912
hg1937912
hg1837912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3716727
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)nsv1048828
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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