A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564155



Internal ID18862436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30496721..30535048hg38UCSC Ensembl
Innerchr18:28076687..28115014hg19UCSC Ensembl
Innerchr18:26330685..26369012hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3838328
hg1938328
hg1838328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056190
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)nssv3564155
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