A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16498059



Internal ID19014933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131482173..131482288hg38UCSC Ensembl
chr6:131803313..131803428hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3676505
Supporting Variants
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)essv16498059
Frequency
Sample Size20
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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