A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608643



Internal ID6995567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33847945..33850775hg38UCSC Ensembl
Innerchr6:33847959..33850761hg38UCSC Ensembl
Outerchr6:33847931..33850789hg38UCSC Ensembl
chr6:33815722..33818552hg19UCSC Ensembl
Innerchr6:33815736..33818538hg19UCSC Ensembl
Outerchr6:33815708..33818566hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382831
hg192831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12311912
SamplesHG03740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608643
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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