A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626657



Internal ID15503504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:112576913..112581808hg38UCSC Ensembl
Outerchr4:113498069..113502964hg19UCSC Ensembl
Outerchr4:113717518..113722413hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg384896
hg194896
hg184896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513161
Supporting Variants
Samples1
Known GenesC4orf21
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626657
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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