A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13946600



Internal ID6145366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118285321..118298180hg38UCSC Ensembl
Innerchr10:118285342..118298159hg38UCSC Ensembl
Outerchr10:118285300..118298201hg38UCSC Ensembl
chr10:120044833..120057692hg19UCSC Ensembl
Innerchr10:120044854..120057671hg19UCSC Ensembl
Outerchr10:120044812..120057713hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3812860
hg1912860
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624686
Supporting Variants
SamplesNA19679
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13946600
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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