A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003313



Internal ID19092532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117347799..117371923hg38UCSC Ensembl
Innerchr3:117066646..117090770hg19UCSC Ensembl
Innerchr3:118549336..118573460hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3824125
hg1924125
hg1824125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735268
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)nsv1003313
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