A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055286



Internal ID18797817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:55613435..55760250hg38UCSC Ensembl
Innerchr18:53280666..53427481hg19UCSC Ensembl
Innerchr18:51431664..51578479hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38146816
hg19146816
hg18146816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726079
Samples
Known GenesTCF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055286
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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