A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10114n54



Internal ID20143538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150777798..150937675hg38UCSC Ensembl
chr5:150157360..150317237hg19UCSC Ensembl
chr5:150137553..150297430hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38159878
hg19159878
hg18159878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599962, nsv599961
Samples
Known GenesIRGM, SMIM3, ZNF300, ZNF300P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10114n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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