A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7861n54



Internal ID19000037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42506833..42514398hg38UCSC Ensembl
chr21:43926943..43934508hg19UCSC Ensembl
chr21:42800012..42807577hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg387566
hg197566
hg187566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv587635, nsv587637
Samples
Known GenesSLC37A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7861n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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