A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021166



Internal ID19110384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48879443..49092264hg38UCSC Ensembl
Innerchr7:48919039..49131860hg19UCSC Ensembl
Innerchr7:48889585..49102406hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38212822
hg19212822
hg18212822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661258, nssv3661259
Samples
Known GenesCDC14C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021166
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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