A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156593



Internal ID22086994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:146810960..146817093hg38UCSC Ensembl
Outerchr6:146810366..146819409hg38UCSC Ensembl
Innerchr6:147132096..147138229hg19UCSC Ensembl
Outerchr6:147131502..147140545hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg389044
hg199044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022697, nssv4022698
Samples
Known GenesADGB
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156593
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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