A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1200e214



Internal ID22757094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87429227..87433611hg38UCSC Ensembl
chr6:88138945..88143329hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384385
hg194385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3609863, esv3609865
SamplesNA20342, NA18879, HG02938, HG03439
Known GenesC6orf165
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1200e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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