A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608434



Internal ID6995363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27658408..27666704hg38UCSC Ensembl
Innerchr6:27658908..27666204hg38UCSC Ensembl
Outerchr6:27657408..27667704hg38UCSC Ensembl
chr6:27626187..27634483hg19UCSC Ensembl
Innerchr6:27626687..27633983hg19UCSC Ensembl
Outerchr6:27625187..27635483hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg388297
hg198297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12238191
SamplesHG01951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608434
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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