A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010815



Internal ID19100032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26491082..26535989hg38UCSC Ensembl
Innerchr3:26532573..26577480hg19UCSC Ensembl
Innerchr3:26507577..26552484hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3844908
hg1944908
hg1844908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4711n100
Supporting Variantsnssv3589543
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)nsv1010815
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