A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609883



Internal ID6996802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88414258..88435959hg38UCSC Ensembl
Innerchr6:88414258..88435959hg38UCSC Ensembl
Outerchr6:88413758..88436459hg38UCSC Ensembl
chr6:89123977..89145678hg19UCSC Ensembl
Innerchr6:89123977..89145678hg19UCSC Ensembl
Outerchr6:89123477..89146178hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3821702
hg1921702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12457604, essv12457603, essv12457605, essv12457601, essv12457602
SamplesNA19669, NA20282, HG02462, HG00553, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609883
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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