A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610318



Internal ID6997235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108369595..108377492hg38UCSC Ensembl
Innerchr6:108369645..108377442hg38UCSC Ensembl
Outerchr6:108369522..108377565hg38UCSC Ensembl
chr6:108690799..108698696hg19UCSC Ensembl
Innerchr6:108690849..108698646hg19UCSC Ensembl
Outerchr6:108690726..108698769hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387898
hg197898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499591, essv12499590
SamplesHG03057, HG03485
Known GenesLACE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610318
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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