A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624406



Internal ID6664573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103167084..103248522hg38UCSC Ensembl
Innerchr10:103167234..103248372hg38UCSC Ensembl
Outerchr10:103166934..103248672hg38UCSC Ensembl
chr10:104926841..105008279hg19UCSC Ensembl
Innerchr10:104926991..105008129hg19UCSC Ensembl
Outerchr10:104926691..105008429hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3881439
hg1981439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913936
SamplesHG02635
Known GenesLOC729020, NT5C2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624406
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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