A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13891393



Internal ID4443647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:90099777..90287576hg38UCSC Ensembl
chr10:91859534..92047333hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38187800
hg19187800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624175
Supporting Variants
SamplesHG03950
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13891393
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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