A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675642



Internal ID9941747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24461307..24461632hg38UCSC Ensembl
chr1:24787797..24788122hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6292877, essv5546110, essv5995185, essv6125001, essv6049949, essv6102526
SamplesNA20294, NA18870, NA18867, NA19707, NA19129, NA20322
Known GenesNIPAL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675642
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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