A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609467



Internal ID6996388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71706900..71707893hg38UCSC Ensembl
Innerchr6:71706922..71707871hg38UCSC Ensembl
Outerchr6:71706878..71707915hg38UCSC Ensembl
chr6:72416603..72417596hg19UCSC Ensembl
Innerchr6:72416625..72417574hg19UCSC Ensembl
Outerchr6:72416581..72417618hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12414488
SamplesHG03642
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609467
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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