A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036958



Internal ID19126177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:30230089..30258154hg38UCSC Ensembl
Innerchr12:30383022..30411087hg19UCSC Ensembl
Innerchr12:30274289..30302354hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3828066
hg1928066
hg1828066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1411n100
Supporting Variantsnssv3505635
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)nsv1036958
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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