A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624466



Internal ID7011321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106286125..106418479hg38UCSC Ensembl
Innerchr10:106286135..106418470hg38UCSC Ensembl
Outerchr10:106286116..106418489hg38UCSC Ensembl
chr10:108045883..108178237hg19UCSC Ensembl
Innerchr10:108045893..108178228hg19UCSC Ensembl
Outerchr10:108045874..108178247hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38132355
hg19132355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13927744
SamplesNA20868
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624466
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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