A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv326n54



Internal ID22768221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73802376..73863685hg38UCSC Ensembl
chr1:74268059..74329368hg19UCSC Ensembl
chr1:74040647..74101956hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3861310
hg1961310
hg1861310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv546573, nsv546574
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv326n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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