A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672534



Internal ID9938639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92771249..92772758hg38UCSC Ensembl
chr15:93314479..93315988hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6464929, essv5516923, essv5776800, essv6009461, essv5746261, essv6060650, essv6351176, essv5467887, essv5595310, essv6485890, essv6164801, essv5402361, essv6372407, essv6198148, essv6148858, essv5838449
SamplesNA19204, NA19350, NA19098, NA18916, NA19404, NA18874, NA19901, NA19189, NA19209, NA19200, NA18912, NA19225, NA19390, NA18909, NA19108, NA19311
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672534
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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