A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060376



Internal ID19149595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:27820466..27987620hg38UCSC Ensembl
Innerchr21:29192785..29359939hg19UCSC Ensembl
Innerchr21:28114656..28281810hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38167155
hg19167155
hg18167155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4422n100
Supporting Variantsnssv3600102
Samples
Known GenesMIR5009
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060376
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