A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565450



Internal ID18863731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51690266..51994459hg38UCSC Ensembl
Innerchr18:49216636..49520829hg19UCSC Ensembl
Innerchr18:47470634..47774827hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38304194
hg19304194
hg18304194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056860
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)nssv3565450
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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