A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv96e199



Internal ID22757869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212853831..212855866hg38UCSC Ensembl
chr1:213027173..213029208hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg382036
hg192036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2663427, esv2659871
SamplesNA19455
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv96e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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