A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12203036



Internal ID3477032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17376471..17381275hg38UCSC Ensembl
Innerchr6:17376971..17380775hg38UCSC Ensembl
Outerchr6:17375471..17382275hg38UCSC Ensembl
chr6:17376702..17381506hg19UCSC Ensembl
Innerchr6:17377202..17381006hg19UCSC Ensembl
Outerchr6:17375702..17382506hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384805
hg194805
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608210
Supporting Variants
SamplesHG03091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12203036
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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