A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611657



Internal ID6651875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167290988..167309829hg38UCSC Ensembl
chr6:167704476..167723317hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3818842
hg1918842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643437, essv12643435, essv12643433, essv12643440, essv12643434, essv12643439, essv12643436, essv12643438
SamplesHG02890, HG02610, HG03241, HG03460, HG02571, HG03428, HG03279, HG03401
Known GenesUNC93A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611657
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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