A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624363



Internal ID6664530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100528312..100531647hg38UCSC Ensembl
Innerchr10:100528354..100531605hg38UCSC Ensembl
Outerchr10:100528270..100531689hg38UCSC Ensembl
chr10:102288069..102291404hg19UCSC Ensembl
Innerchr10:102288111..102291362hg19UCSC Ensembl
Outerchr10:102288027..102291446hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg383336
hg193336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13912978
SamplesHG02702
Known GenesNDUFB8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624363
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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