A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663301



Internal ID9929406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90247103..90247856hg38UCSC Ensembl
chr15:90790335..90791088hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5410626, essv6057708, essv5460368, essv6201783, essv6052865, essv5824814, essv5437779, essv6568136, essv6096193, essv6224453, essv5825930, essv5540560, essv6093264, essv6285923, essv6550177
SamplesNA18486, NA19377, NA19197, NA19138, NA19384, HG01080, NA19451, HG01171, HG01102, NA19436, NA20281, NA19818, NA19713, NA19116, NA19463
Known GenesCIB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663301
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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