A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998580



Internal ID18811430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111816..138468hg38UCSC Ensembl
Innerchr3:153499..180151hg19UCSC Ensembl
Innerchr3:128499..155151hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3826653
hg1926653
hg1826653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590265
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)nsv998580
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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