A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3666805



Internal ID19384813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142836927..142836927hg38UCSC Ensembl
chr4:143758080..143758080hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16489328
Samples
Known GenesINPP4B
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)esv3666805
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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