A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661102



Internal ID9580521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162321869..162323900hg38UCSC Ensembl
chr2:163178379..163180410hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382032
hg192032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6529863, essv5791377, essv6004006, essv5459757, essv5920017, essv5833509, essv6194616, essv6102921, essv5904272, essv6229914
SamplesNA19397, NA19359, NA18504, NA19908, NA19436, NA19375, NA19428, NA19467, NA19376, NA19116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661102
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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