A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585205



Internal ID6972729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10894194..10896062hg38UCSC Ensembl
Innerchr1:10894198..10896058hg38UCSC Ensembl
Outerchr1:10894190..10896066hg38UCSC Ensembl
chr1:10954251..10956119hg19UCSC Ensembl
Innerchr1:10954255..10956115hg19UCSC Ensembl
Outerchr1:10954247..10956123hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381869
hg191869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9853316, essv9853317, essv9853330, essv9853338, essv9853337, essv9853326, essv9853324, essv9853323, essv9853319, essv9853321, essv9853318, essv9853334, essv9853332, essv9853333, essv9853331, essv9853341, essv9853329, essv9853322, essv9853320, essv9853325, essv9853340, essv9853327, essv9853339, essv9853328, essv9853336, essv9853335
SamplesNA20882, HG01441, HG01188, HG00257, HG03015, HG00640, HG00327, HG03235, HG03673, HG03234, HG02490, NA20896, HG01248, NA20876, HG04235, HG01047, HG01762, NA21086, HG01286, HG03869, NA20544, NA21102, HG02348, NA20827, HG03985, HG00255
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585205
Frequency
Sample Size2504
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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