A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13908847



Internal ID4800450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97813909..97825255hg38UCSC Ensembl
Innerchr10:97814059..97825105hg38UCSC Ensembl
Outerchr10:97813759..97825405hg38UCSC Ensembl
chr10:99573666..99585012hg19UCSC Ensembl
Innerchr10:99573816..99584862hg19UCSC Ensembl
Outerchr10:99573516..99585162hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3811347
hg1911347
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624324
Supporting Variants
SamplesNA11933
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13908847
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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