A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv16n21



Internal ID20131737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119039277..119046720hg38UCSC Ensembl
chr1:119581900..119589343hg19UCSC Ensembl
chr1:119383423..119390866hg18UCSC Ensembl
chr1:119293942..119301385hg17UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg387444
hg197444
hg187444
hg177444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517843, nsv517011
Samples
Known GenesWARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv16n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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