A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609779



Internal ID6996699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83533782..83550762hg38UCSC Ensembl
Innerchr6:83533832..83550712hg38UCSC Ensembl
Outerchr6:83533720..83550824hg38UCSC Ensembl
chr6:84243501..84260481hg19UCSC Ensembl
Innerchr6:84243551..84260431hg19UCSC Ensembl
Outerchr6:84243439..84260543hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg3816981
hg1916981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1198e214
Supporting Variantsessv12454001
SamplesHG02614
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609779
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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