A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009521



Internal ID19098739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:20110718..20189198hg38UCSC Ensembl
Innerchr2:20310479..20388959hg19UCSC Ensembl
Innerchr2:20173960..20252440hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3878481
hg1978481
hg1878481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3578987
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)nsv1009521
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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