A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008961



Internal ID19098179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3794109..3831369hg38UCSC Ensembl
Innerchr2:3841699..3878959hg19UCSC Ensembl
Innerchr2:3819574..3856834hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3837261
hg1937261
hg1837261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3571302
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)nsv1008961
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