A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16466636



Internal ID19330196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25929822..25930157hg38UCSC Ensembl
chrX:25947939..25948274hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3674941
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)essv16466636
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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