A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046565



Internal ID19135784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33099232..33141714hg38UCSC Ensembl
Innerchr12:33252166..33294648hg19UCSC Ensembl
Innerchr12:33143433..33185915hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3842483
hg1942483
hg1842483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514188
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)nsv1046565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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