A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156553



Internal ID22086954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80574472..80579817hg38UCSC Ensembl
Outerchr6:80568270..80584624hg38UCSC Ensembl
Innerchr6:81284189..81289534hg19UCSC Ensembl
Outerchr6:81277987..81294341hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816355
hg1916355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv253n97
Supporting Variantsnssv4021732, nssv4021746, nssv4021738, nssv4021748, nssv4021745, nssv4021742, nssv4021739, nssv4021736, nssv4021733, nssv4021731, nssv4021737, nssv4021734, nssv4021740, nssv4021735, nssv4021749, nssv4021743, nssv4021747, nssv4021744, nssv4021750, nssv4021741
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156553
Frequency
Sample Size131
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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