A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045515



Internal ID19134734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:98010688..98133763hg38UCSC Ensembl
Innerchr12:98404466..98527541hg19UCSC Ensembl
Innerchr12:96928597..97051672hg18UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38123076
hg19123076
hg18123076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524845
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)nsv1045515
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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