A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13676421



Internal ID3678237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3072358..3073773hg38UCSC Ensembl
Innerchr10:3072365..3073766hg38UCSC Ensembl
Outerchr10:3072351..3073780hg38UCSC Ensembl
chr10:3114550..3115965hg19UCSC Ensembl
Innerchr10:3114557..3115958hg19UCSC Ensembl
Outerchr10:3114543..3115972hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622161
Supporting Variants
SamplesHG03882
Known GenesPFKP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13676421
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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