A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037780



Internal ID19126999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:125906783..125931200hg38UCSC Ensembl
Innerchr12:126391329..126415746hg19UCSC Ensembl
Innerchr12:124957282..124981699hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3824418
hg1924418
hg1824418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1569n100
Supporting Variantsnssv3526127
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)nsv1037780
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer