A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv31e199



Internal ID22757804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24569169..24574377hg38UCSC Ensembl
chr1:24895660..24900868hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385209
hg195209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2676241, esv2675930
SamplesNA18924, NA19466, NA19204, NA18508, NA19704, NA18486, NA19098, NA19313, NA18498, NA18874, NA19235, NA19207, NA19172, NA19210, NA19152, NA18933, NA18910, HG01390, NA19654, NA19449, NA18912, NA18853, NA19395, NA19436, NA19834, NA19331, NA19311, NA19711, NA18505, NA18511, NA18522, NA18487
Known GenesNCMAP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv31e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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