A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13704096



Internal ID3705912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15367490..15486645hg38UCSC Ensembl
chr10:15409489..15528644hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38119156
hg19119156
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622442
Supporting Variants
SamplesHG01796
Known GenesFAM171A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13704096
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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