A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770332



Internal ID6749403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45256785..45257514hg38UCSC Ensembl
Innerchr10:45256785..45257514hg38UCSC Ensembl
Outerchr10:45256464..45257812hg38UCSC Ensembl
chr10:45752233..45752962hg19UCSC Ensembl
Innerchr10:45752233..45752962hg19UCSC Ensembl
Outerchr10:45751912..45753260hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623090
Supporting Variants
SamplesNA20864
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770332
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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