A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156578



Internal ID22086979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121639714..121649281hg38UCSC Ensembl
Outerchr6:121635557..121654417hg38UCSC Ensembl
Innerchr6:121960860..121970427hg19UCSC Ensembl
Outerchr6:121956703..121975563hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3818861
hg1918861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv257n97
Supporting Variantsnssv4022628
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156578
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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