A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021647



Internal ID19110865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20064069..20152671hg38UCSC Ensembl
Innerchr9:20064067..20152669hg19UCSC Ensembl
Innerchr9:20054067..20142669hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3888603
hg1988603
hg1888603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690697
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021647
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