A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16500898



Internal ID19364458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102491858..102492164hg38UCSC Ensembl
chr10:104251615..104251921hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3679659
Supporting Variants
Samples
Known GenesACTR1A
MethodSequencing
Analysisde novo assemblies produced from SoapDenovo2 were aligned to GRC37 using LAST and input into SoapAsmVar for population-wide structural variation detection. The method is described in the publication
PlatformIllumina HiSeq 2000
Comments
ReferenceBesenbacher_et_al_2015
Pubmed ID25597990
Accession Number(s)essv16500898
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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