A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13866601



Internal ID3287551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77864092..77866940hg38UCSC Ensembl
Innerchr10:77864094..77866939hg38UCSC Ensembl
Outerchr10:77864091..77866942hg38UCSC Ensembl
chr10:79623850..79626698hg19UCSC Ensembl
Innerchr10:79623852..79626697hg19UCSC Ensembl
Outerchr10:79623849..79626700hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382849
hg192849
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623883
Supporting Variants
SamplesHG02922
Known GenesDLG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13866601
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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