A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626584



Internal ID15503431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184158560..184161350hg38UCSC Ensembl
Outerchr3:183876348..183879138hg19UCSC Ensembl
Outerchr3:185359042..185361832hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg382791
hg192791
hg182791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513096
Supporting Variants
Samples1
Known GenesDVL3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626584
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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