A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039826



Internal ID18782357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:1150665..1374160hg38UCSC Ensembl
Innerchr12:1259831..1483326hg19UCSC Ensembl
Innerchr12:1130092..1353587hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38223496
hg19223496
hg18223496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509578
Samples
Known GenesERC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039826
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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