A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12232687



Internal ID4870396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26192794..26212452hg38UCSC Ensembl
Innerchr6:26193294..26211952hg38UCSC Ensembl
Outerchr6:26191794..26213452hg38UCSC Ensembl
chr6:26193022..26212680hg19UCSC Ensembl
Innerchr6:26193522..26212180hg19UCSC Ensembl
Outerchr6:26192022..26213680hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3819659
hg1919659
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608397
Supporting Variants
SamplesNA12340
Known GenesHIST1H2AD, HIST1H2BF, HIST1H3D, HIST1H4E
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12232687
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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