A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596153



Internal ID18894434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75434082..75497567hg38UCSC Ensembl
Innerchr3:75483233..75546718hg19UCSC Ensembl
Innerchr3:75565923..75629408hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3863486
hg1963486
hg1863486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013299
Supporting Variants
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596153
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