A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3662321



Internal ID19380329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71358177..71358177hg38UCSC Ensembl
chrX:70578027..70578027hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16485293
Samples
Known GenesBCYRN1
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)esv3662321
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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