A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv663e214



Internal ID22756557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43035486..43105414hg38UCSC Ensembl
chr19:43539638..43609566hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3869929
hg1969929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644440, esv3644439
SamplesNA12842, NA19397, HG03163, NA20274, HG01815, HG03449, NA18999, HG02891, HG03455, NA12058, HG03792, NA20517, HG03069, NA12155, HG03074, HG01350, HG01325, HG02153, HG01366, NA20774, NA19916, HG03673, HG01354, NA18498, HG01110, HG03209, HG02143, HG02561, HG02315, NA18874, NA20775, HG02573, HG01519, HG02471, HG01048, HG03583, HG02409, HG04075, HG02479, HG00176, HG03547, HG01882, HG02554, HG02144, HG00320, NA18630, HG03301, HG02429, NA18856, HG02649, NA19338, HG01936, NA19625, HG03064, NA19375, NA21113, NA18542, HG02667, NA19834, NA18543, NA19256, NA19147, NA20276, NA20792, HG02941, HG01620, HG01798, NA19376, NA18501, HG02052, HG01883, HG01082, HG02284, NA18522, HG02406, HG00255
Known GenesPSG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv663e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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