A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3665921



Internal ID19037243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24548140..24548140hg38UCSC Ensembl
chr4:24549763..24549763hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16488532
Samples
Known GenesDHX15
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)esv3665921
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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