A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035561



Internal ID19124780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30135946..30183553hg38UCSC Ensembl
Innerchr12:30288879..30336486hg19UCSC Ensembl
Innerchr12:30180146..30227753hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3847608
hg1947608
hg1847608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1409n100
Supporting Variantsnssv3710340
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)nsv1035561
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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