A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053524



Internal ID19142743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33136012..33170417hg38UCSC Ensembl
Innerchr12:33288946..33323351hg19UCSC Ensembl
Innerchr12:33180213..33214618hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3834406
hg1934406
hg1834406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522563
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)nsv1053524
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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