A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155462



Internal ID22085967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33541751..33550679hg38UCSC Ensembl
Outerchr1:33538376..33552421hg38UCSC Ensembl
Innerchr1:34007351..34016279hg19UCSC Ensembl
Outerchr1:34003976..34018021hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3814046
hg1914046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012215
Samples
Known GenesCSMD2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155462
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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