A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035837



Internal ID19125056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31846060..31910068hg38UCSC Ensembl
Innerchr12:31998994..32063002hg19UCSC Ensembl
Innerchr12:31890261..31954269hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3864009
hg1964009
hg1864009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1426n100
Supporting Variantsnssv3516848, nssv3513067, nssv3506435, nssv3711309, nssv3511740
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)nsv1035837
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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