A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675930



Internal ID9942035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24569169..24574294hg38UCSC Ensembl
chr1:24895660..24900785hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385126
hg195126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv31e199
Supporting Variantsessv6420149, essv6269137, essv5977065, essv6055536, essv5451889, essv5961826, essv6515692, essv5654494, essv6325727, essv6177306, essv6017678, essv6484731, essv5438315, essv6509219
SamplesNA19204, NA18508, NA18486, NA19098, NA18498, NA19207, NA19172, NA19210, NA19152, NA18912, NA18853, NA18505, NA18511, NA18522
Known GenesNCMAP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675930
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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