A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770337



Internal ID3750131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45502562..45515588hg38UCSC Ensembl
Innerchr10:45502562..45515588hg38UCSC Ensembl
Outerchr10:45502062..45516088hg38UCSC Ensembl
chr10:45998010..46011036hg19UCSC Ensembl
Innerchr10:45998010..46011036hg19UCSC Ensembl
Outerchr10:45997510..46011536hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813027
hg1913027
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623095
Supporting Variants
SamplesHG03380
Known GenesMARCH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770337
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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