A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036000



Internal ID19125219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:2964853..3039074hg38UCSC Ensembl
Innerchr12:3074019..3148240hg19UCSC Ensembl
Innerchr12:2944280..3018501hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3874222
hg1974222
hg1874222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503234
Samples
Known GenesTEAD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036000
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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