A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035259



Internal ID19124478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60614415..60701473hg38UCSC Ensembl
Innerchr12:61008196..61095254hg19UCSC Ensembl
Innerchr12:59294463..59381521hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3887059
hg1987059
hg1887059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1510n100
Supporting Variantsnssv3523639, nssv3523640, nssv3523638, nssv3523641, nssv3523642
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)nsv1035259
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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