A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016754



Internal ID18759289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165863651..165905512hg38UCSC Ensembl
Innerchr4:166784803..166826664hg19UCSC Ensembl
Innerchr4:167004253..167046114hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3841862
hg1941862
hg1841862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634170
Samples
Known GenesTLL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016754
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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