A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16485538



Internal ID19002412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115482236..115482236hg38UCSC Ensembl
chrX:114716605..114716605hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3662594
Supporting Variants
Samples
Known Genes
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)essv16485538
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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