A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564219



Internal ID18862500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39636758..39682665hg38UCSC Ensembl
Innerchr18:37216722..37262629hg19UCSC Ensembl
Innerchr18:35470720..35516627hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3845908
hg1945908
hg1845908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064182
Supporting Variants
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564219
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