A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565368



Internal ID18863649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43857645..43901624hg38UCSC Ensembl
Innerchr18:41437610..41481589hg19UCSC Ensembl
Innerchr18:39691608..39735587hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3843980
hg1943980
hg1843980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064666
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)nssv3565368
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