A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035958



Internal ID19125177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9319769..9426513hg38UCSC Ensembl
Innerchr12:9472365..9579109hg19UCSC Ensembl
Innerchr12:9363632..9470376hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38106745
hg19106745
hg18106745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503198
Samples
Known GenesDDX12P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035958
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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