A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13745982



Internal ID3226580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30721211..30770896hg38UCSC Ensembl
Innerchr10:30721211..30770896hg38UCSC Ensembl
Outerchr10:30720711..30771396hg38UCSC Ensembl
chr10:31010140..31059825hg19UCSC Ensembl
Innerchr10:31010140..31059825hg19UCSC Ensembl
Outerchr10:31009640..31060325hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3849686
hg1949686
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622795
Supporting Variants
SamplesHG02837
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13745982
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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