A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3662038



Internal ID19380046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31018137..31018137hg38UCSC Ensembl
chrX:31036254..31036254hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16485038
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)esv3662038
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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