A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609915



Internal ID6996834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90096164..90100075hg38UCSC Ensembl
Innerchr6:90096171..90100068hg38UCSC Ensembl
Outerchr6:90096157..90100082hg38UCSC Ensembl
chr6:90805883..90809794hg19UCSC Ensembl
Innerchr6:90805890..90809787hg19UCSC Ensembl
Outerchr6:90805876..90809801hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383912
hg193912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12460045, essv12460044
SamplesHG03539, HG02010
Known GenesBACH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609915
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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