A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16485634



Internal ID19002508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130146518..130146518hg38UCSC Ensembl
chrX:129280493..129280493hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3662701
Supporting Variants
Samples
Known GenesAIFM1
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)essv16485634
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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