A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056860



Internal ID19146079
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 StatusM
Merged Variants
Supporting Variantsnssv3565450
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)nsv1056860
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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