A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156131



Internal ID22086636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:777165..901705hg38UCSC Ensembl
Outerchr1:771719..914637hg38UCSC Ensembl
Innerchr1:712545..837085hg19UCSC Ensembl
Outerchr1:707099..850017hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38142919
hg19142919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017941
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100288069
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156131
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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