A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3662937



Internal ID19380945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15426584..15426584hg38UCSC Ensembl
chrY:17538464..17538464hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16485847
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)esv3662937
Frequency
Sample Size20
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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