A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033406



Internal ID19122628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14218572..14255120hg38UCSC Ensembl
Innerchr7:14258197..14294745hg19UCSC Ensembl
Innerchr7:14224722..14261270hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3836549
hg1936549
hg1836549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643156
Samples
Known GenesDGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033406
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