A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037270



Internal ID19126489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31128312..31242897hg38UCSC Ensembl
Innerchr12:31281246..31395831hg19UCSC Ensembl
Innerchr12:31172513..31287098hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38114586
hg19114586
hg18114586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1419n100
Supporting Variantsnssv3519551, nssv3514844
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)nsv1037270
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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