A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002791



Internal ID19092008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41712569..41738598hg38UCSC Ensembl
Innerchr2:41939709..41965738hg19UCSC Ensembl
Innerchr2:41793213..41819242hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3826030
hg1926030
hg1826030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581567
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)nsv1002791
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