A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13749849



Internal ID1276487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31985116..31996140hg38UCSC Ensembl
chr10:32274044..32285068hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3811025
hg1911025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622823
Supporting Variants
SamplesHG01122
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13749849
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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