A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059347



Internal ID19148566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1907315..1973670hg38UCSC Ensembl
Innerchr18:1907316..1973671hg19UCSC Ensembl
Innerchr18:1897316..1963671hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3866356
hg1966356
hg1866356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3564025, nssv3564026, nssv3564023, nssv3564024
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)nsv1059347
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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