A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624442



Internal ID15847978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:99586587..99587639hg38UCSC Ensembl
Outerchr6:100034463..100035515hg19UCSC Ensembl
Outerchr6:100141184..100142236hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg381053
hg191053
hg181053
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511907
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624442
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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