A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565455



Internal ID18863736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56537922..56577451hg38UCSC Ensembl
Innerchr18:54205153..54244682hg19UCSC Ensembl
Innerchr18:52356151..52395680hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3839530
hg1939530
hg1839530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058641
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)nssv3565455
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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