A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564205



Internal ID18862486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36959202..37006782hg38UCSC Ensembl
Innerchr18:34539165..34586745hg19UCSC Ensembl
Innerchr18:32793163..32840743hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3847581
hg1947581
hg1847581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059592
Supporting Variants
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564205
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