A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059026



Internal ID19148245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:5676697..5805052hg38UCSC Ensembl
Innerchr18:5676696..5805051hg19UCSC Ensembl
Innerchr18:5666696..5795051hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38128356
hg19128356
hg18128356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564081
Samples
Known GenesLOC645355
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059026
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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