A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545658



Internal ID18843939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27674339..27696482hg38UCSC Ensembl
Innerchr15:27919485..27941628hg19UCSC Ensembl
Innerchr15:25593080..25615223hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3822144
hg1922144
hg1822144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035878
Supporting Variants
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)nssv3545658
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