A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13803446



Internal ID3805262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50879906..50917614hg38UCSC Ensembl
Innerchr10:50879945..50917576hg38UCSC Ensembl
Outerchr10:50879868..50917653hg38UCSC Ensembl
chr10:52639666..52677374hg19UCSC Ensembl
Innerchr10:52639705..52677336hg19UCSC Ensembl
Outerchr10:52639628..52677413hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3837709
hg1937709
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623217
Supporting Variants
SamplesHG02054
Known GenesA1CF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13803446
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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