A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3676786



Internal ID19394794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85494999..85495090hg38UCSC Ensembl
chrX:84750004..84750095hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16466802
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)esv3676786
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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