A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13153634



Internal ID6181689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29678818..29679122hg38UCSC Ensembl
Innerchr8:29678824..29679116hg38UCSC Ensembl
Outerchr8:29678812..29679128hg38UCSC Ensembl
chr8:29536334..29536638hg19UCSC Ensembl
Innerchr8:29536340..29536632hg19UCSC Ensembl
Outerchr8:29536328..29536644hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616774
Supporting Variants
SamplesNA19717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13153634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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