A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156570



Internal ID22086971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110068666..110092034hg38UCSC Ensembl
Outerchr6:110065139..110094225hg38UCSC Ensembl
Innerchr6:110389869..110413237hg19UCSC Ensembl
Outerchr6:110386342..110415428hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3829087
hg1929087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv256n97
Supporting Variantsnssv4022619
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156570
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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