A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13970259



Internal ID3192305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127755197..127791540hg38UCSC Ensembl
Innerchr10:127755197..127791540hg38UCSC Ensembl
Outerchr10:127754697..127792040hg38UCSC Ensembl
chr10:129553461..129589804hg19UCSC Ensembl
Innerchr10:129553461..129589804hg19UCSC Ensembl
Outerchr10:129552961..129590304hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3836344
hg1936344
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624890
Supporting Variants
SamplesHG02805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13970259
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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