A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156531



Internal ID22086932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76303839..76318064hg38UCSC Ensembl
Outerchr6:76294154..76323236hg38UCSC Ensembl
Innerchr6:77013556..77027781hg19UCSC Ensembl
Outerchr6:77003871..77032953hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3829083
hg1929083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021620, nssv4021619
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156531
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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