A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156462



Internal ID22086863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24958279..24968454hg38UCSC Ensembl
Outerchr6:24957283..24971493hg38UCSC Ensembl
Innerchr6:24958507..24968682hg19UCSC Ensembl
Outerchr6:24957511..24971721hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3814211
hg1914211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018317
Samples
Known GenesFAM65B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156462
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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