A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051343



Internal ID19140562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73906179..74030129hg38UCSC Ensembl
Innerchr12:74299959..74423909hg19UCSC Ensembl
Innerchr12:72586226..72710176hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38123951
hg19123951
hg18123951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1527n100
Supporting Variantsnssv3712551
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)nsv1051343
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