A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913936



Internal ID3915752
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624406
Supporting Variants
SamplesHG02635
Known GenesLOC729020, NT5C2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913936
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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