A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624855



Internal ID15848391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:129145506..129147103hg38UCSC Ensembl
Outerchr4:129139075..129151497hg38UCSC Ensembl
Innerchr4:130066661..130068258hg19UCSC Ensembl
Outerchr4:130060230..130072652hg19UCSC Ensembl
Innerchr4:130286111..130287708hg18UCSC Ensembl
Outerchr4:130279680..130292102hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3812423
hg1912423
hg1812423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511266
Supporting Variants
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624855
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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