A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608186



Internal ID6995116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16042623..16043887hg38UCSC Ensembl
Innerchr6:16042623..16043887hg38UCSC Ensembl
Outerchr6:16042426..16044178hg38UCSC Ensembl
chr6:16042854..16044118hg19UCSC Ensembl
Innerchr6:16042854..16044118hg19UCSC Ensembl
Outerchr6:16042657..16044409hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381265
hg191265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12200605, essv12200609, essv12200608, essv12200607, essv12200602, essv12200603, essv12200606, essv12200604
SamplesNA21115, HG03679, NA20894, NA20910, HG01512, NA20856, NA20528, HG01507
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608186
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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