A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566443



Internal ID18864724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67592968..68009670hg38UCSC Ensembl
Innerchr18:65260205..65676907hg19UCSC Ensembl
Innerchr18:63411185..63827887hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38416703
hg19416703
hg18416703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063370
Supporting Variants
Samples
Known GenesLOC643542
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566443
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