A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666403



Internal ID9585822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3702090..3703982hg38UCSC Ensembl
chr16:3752091..3753983hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381893
hg191893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6198370, essv6513106, essv6592627, essv5948546, essv5666214, essv5606263, essv5925216, essv6552831, essv6545880, essv5682067
SamplesNA19207, NA18870, NA18868, NA19982, NA19908, NA19380, NA19382, NA18907, NA19399, NA19448
Known GenesTRAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666403
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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