A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv662e214



Internal ID22756556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43003765..43279474hg38UCSC Ensembl
chr19:43507917..43783626hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38275710
hg19275710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644442, esv3644437
SamplesHG03163, NA20274, HG03449, NA18999, HG02891, HG03455, NA20517, HG03069, HG03074, HG01350, HG01366, NA20774, NA19916, NA18498, HG01110, HG03209, HG02143, HG02561, HG02315, NA18874, NA20775, HG02573, HG02471, HG03583, HG04075, HG03547, HG01882, HG02554, HG02144, NA18856, HG02649, NA19338, HG01936, NA19625, HG03064, NA21113, HG02667, NA19834, NA18543, NA19256, NA19147, NA20276, HG02941, HG01620, NA18501, HG02052, HG01883, HG02284, NA18522
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv662e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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