A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608189



Internal ID6995119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16178589..16189480hg38UCSC Ensembl
Innerchr6:16178593..16189476hg38UCSC Ensembl
Outerchr6:16178585..16189484hg38UCSC Ensembl
chr6:16178820..16189711hg19UCSC Ensembl
Innerchr6:16178824..16189707hg19UCSC Ensembl
Outerchr6:16178816..16189715hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810892
hg1910892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12200612
SamplesHG02690
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608189
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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