A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv37n54



Internal ID22767932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1663759..1696548hg38UCSC Ensembl
chr1:1595198..1627987hg19UCSC Ensembl
chr1:1585061..1617847hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3832790
hg1932790
hg1832787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv545024, nsv545025, nsv545019, nsv545023
Samples
Known GenesCDK11B, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv37n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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