A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998862



Internal ID19158399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25936901..26075136hg38UCSC Ensembl
Innerchr3:25978392..26116627hg19UCSC Ensembl
Innerchr3:25953396..26091631hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38138236
hg19138236
hg18138236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589517
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)nsv998862
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