A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13784850



Internal ID3786666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46399372..46400990hg38UCSC Ensembl
Innerchr10:46399388..46400973hg38UCSC Ensembl
Outerchr10:46399355..46401006hg38UCSC Ensembl
chr10:47148773..47150391hg19UCSC Ensembl
Innerchr10:47148790..47150375hg19UCSC Ensembl
Outerchr10:47148757..47150408hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381619
hg191619
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623121
Supporting Variants
SamplesHG03401
Known GenesLINC00842
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13784850
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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