A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13712286



Internal ID6016108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19536634..19746769hg38UCSC Ensembl
chr10:19825563..20035698hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38210136
hg19210136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622540
Supporting Variants
SamplesNA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13712286
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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