A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659098



Internal ID9925203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:25960374..25960473hg38UCSC Ensembl
Outerchr2:25960337..25960523hg38UCSC Ensembl
Innerchr2:26183243..26183342hg19UCSC Ensembl
Outerchr2:26183206..26183392hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6400151, essv5567355, essv6000880, essv5649952, essv6258630
SamplesHG01060, HG00257, HG01069, HG00260, NA11831
Known GenesKIF3C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659098
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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