A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511613



Internal ID15851038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52385367..52387866hg38UCSC Ensembl
Outerchr19:52384818..52391913hg38UCSC Ensembl
Innerchr19:52888620..52891119hg19UCSC Ensembl
Outerchr19:52888071..52895166hg19UCSC Ensembl
Innerchr19:57580432..57582931hg18UCSC Ensembl
Outerchr19:57579883..57586978hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg387096
hg197096
hg187096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626244
Samples1
Known GenesZNF880
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511613
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer