A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13153553



Internal ID4089841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29610934..29617840hg38UCSC Ensembl
Innerchr8:29610943..29617832hg38UCSC Ensembl
Outerchr8:29610926..29617849hg38UCSC Ensembl
chr8:29468450..29475356hg19UCSC Ensembl
Innerchr8:29468459..29475348hg19UCSC Ensembl
Outerchr8:29468442..29475365hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386907
hg196907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616769
Supporting Variants
SamplesHG03716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13153553
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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