A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16466571



Internal ID19330131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104227865..104227928hg38UCSC Ensembl
chr10:105987623..105987686hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3674219
Supporting Variants
Samples
Known GenesWDR96
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)essv16466571
Frequency
Sample Size20
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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