A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2n21



Internal ID22766194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5564469..5565506hg38UCSC Ensembl
chr1:5624529..5625566hg19UCSC Ensembl
chr1:5547116..5548153hg18UCSC Ensembl
chr1:5558795..5559832hg17UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381038
hg191038
hg181038
hg171038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526005, nsv519513
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv2n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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