A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611206



Internal ID6998117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149355626..149364593hg38UCSC Ensembl
Innerchr6:149355626..149364593hg38UCSC Ensembl
Outerchr6:149355552..149364702hg38UCSC Ensembl
chr6:149676762..149685729hg19UCSC Ensembl
Innerchr6:149676762..149685729hg19UCSC Ensembl
Outerchr6:149676688..149685838hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388968
hg198968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12580808
SamplesNA19093
Known GenesTAB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611206
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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