A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609814



Internal ID6996733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85333437..85406449hg38UCSC Ensembl
Innerchr6:85333437..85406449hg38UCSC Ensembl
Outerchr6:85332937..85406949hg38UCSC Ensembl
chr6:86043155..86116167hg19UCSC Ensembl
Innerchr6:86043155..86116167hg19UCSC Ensembl
Outerchr6:86042655..86116667hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3873013
hg1973013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12454831
SamplesNA19472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609814
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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