A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622188



Internal ID6662358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4212250..4213767hg38UCSC Ensembl
Innerchr10:4212250..4213767hg38UCSC Ensembl
Outerchr10:4212189..4214122hg38UCSC Ensembl
chr10:4254442..4255959hg19UCSC Ensembl
Innerchr10:4254442..4255959hg19UCSC Ensembl
Outerchr10:4254381..4256314hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13680689
SamplesHG02938
Known GenesLINC00702
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622188
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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