A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12461651



Internal ID3091299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90877893..90881391hg38UCSC Ensembl
Innerchr6:90877893..90881391hg38UCSC Ensembl
Outerchr6:90877646..90881595hg38UCSC Ensembl
chr6:91587611..91591109hg19UCSC Ensembl
Innerchr6:91587611..91591109hg19UCSC Ensembl
Outerchr6:91587364..91591313hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383499
hg193499
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609929
Supporting Variants
SamplesHG02716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12461651
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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