A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13912975



Internal ID5660093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100432148..100452126hg38UCSC Ensembl
Innerchr10:100432148..100452126hg38UCSC Ensembl
Outerchr10:100432067..100452203hg38UCSC Ensembl
chr10:102191905..102211883hg19UCSC Ensembl
Innerchr10:102191905..102211883hg19UCSC Ensembl
Outerchr10:102191824..102211960hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3819979
hg1919979
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624360
Supporting Variants
SamplesNA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13912975
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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