A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13737833



Internal ID3739649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28275692..28283742hg38UCSC Ensembl
Innerchr10:28275692..28283742hg38UCSC Ensembl
Outerchr10:28275332..28284121hg38UCSC Ensembl
chr10:28564621..28572671hg19UCSC Ensembl
Innerchr10:28564621..28572671hg19UCSC Ensembl
Outerchr10:28564261..28573050hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388051
hg198051
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622742
Supporting Variants
SamplesHG03123
Known GenesMPP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13737833
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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