A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156504



Internal ID22086905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54983657..54985344hg38UCSC Ensembl
Outerchr6:54980887..54987314hg38UCSC Ensembl
Innerchr6:54848455..54850142hg19UCSC Ensembl
Outerchr6:54845685..54852112hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg386428
hg196428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018586, nssv4018590, nssv4018587, nssv4018588, nssv4018589
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156504
Frequency
Sample Size131
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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