A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6400151



Internal ID8818114
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 StatusS
Merged Variantsesv2659098
Supporting Variants
SamplesHG00260
Known GenesKIF3C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6400151
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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