A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913052



Internal ID1150575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101283105..101284940hg38UCSC Ensembl
Innerchr10:101283105..101284940hg38UCSC Ensembl
Outerchr10:101282782..101285348hg38UCSC Ensembl
chr10:103042862..103044697hg19UCSC Ensembl
Innerchr10:103042862..103044697hg19UCSC Ensembl
Outerchr10:103042539..103045105hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624374
Supporting Variants
SamplesHG01028
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913052
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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