A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021771



Internal ID18764305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22279864..22419061hg38UCSC Ensembl
Innerchr6:22280093..22419290hg19UCSC Ensembl
Innerchr6:22388072..22527269hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38139198
hg19139198
hg18139198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5924n100
Supporting Variantsnssv3749043
Samples
Known GenesPRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021771
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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