A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1165e214



Internal ID20122588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10521953..10553306hg38UCSC Ensembl
chr6:10522186..10553539hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3831354
hg1931354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3608077, esv3608076
SamplesHG03857, HG02292, HG00611
Known GenesGCNT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1165e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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