A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035759



Internal ID19124978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31849350..31915943hg38UCSC Ensembl
Innerchr12:32002284..32068877hg19UCSC Ensembl
Innerchr12:31893551..31960144hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3866594
hg1966594
hg1866594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1426n100
Supporting Variantsnssv3518027, nssv3519647, nssv3505449, nssv3516011, nssv3512072, nssv3712414, nssv3518959, nssv3506273, nssv3712413, nssv3505816, nssv3504244, nssv3521961
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)nsv1035759
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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