A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626798



Internal ID15850331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141853345..141854006hg38UCSC Ensembl
Outerchr3:141853201..141854919hg38UCSC Ensembl
Innerchr3:141572187..141572848hg19UCSC Ensembl
Outerchr3:141572043..141573761hg19UCSC Ensembl
Innerchr3:143054877..143055538hg18UCSC Ensembl
Outerchr3:143054733..143056451hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381719
hg191719
hg181719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511222
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)nssv626798
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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