A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040887



Internal ID19130106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12539061..12556390hg38UCSC Ensembl
Innerchr16:12632918..12650247hg19UCSC Ensembl
Innerchr16:12540419..12557748hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3817330
hg1917330
hg1817330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2731n100
Supporting Variantsnssv3557158, nssv3557156, nssv3557157
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040887
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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