A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608328



Internal ID6995258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22090990..22126849hg38UCSC Ensembl
Innerchr6:22091000..22126839hg38UCSC Ensembl
Outerchr6:22090980..22126859hg38UCSC Ensembl
chr6:22091219..22127078hg19UCSC Ensembl
Innerchr6:22091229..22127068hg19UCSC Ensembl
Outerchr6:22091209..22127088hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3835860
hg1935860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12222933
SamplesHG02601
Known GenesCASC15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608328
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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