A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037378



Internal ID18779909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31104761..31259280hg38UCSC Ensembl
Innerchr12:31257695..31412214hg19UCSC Ensembl
Innerchr12:31148962..31303481hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38154520
hg19154520
hg18154520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n100
Supporting Variantsnssv3503829
Samples
Known GenesDDX11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037378
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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