A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609268



Internal ID6996190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63784656..63787201hg38UCSC Ensembl
Innerchr6:63784656..63787201hg38UCSC Ensembl
Outerchr6:63784434..63787373hg38UCSC Ensembl
chr6:64494549..64497094hg19UCSC Ensembl
Innerchr6:64494549..64497094hg19UCSC Ensembl
Outerchr6:64494327..64497266hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382546
hg192546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389911, essv12389917, essv12389914, essv12389912, essv12389913, essv12389916, essv12389915
SamplesHG03190, HG03352, NA18908, NA19913, NA20276, HG02308, NA19116
Known GenesEYS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609268
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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