A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154973



Internal ID22085478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110021263..110022852hg38UCSC Ensembl
Outerchr13:110020621..110026428hg38UCSC Ensembl
Innerchr13:110673610..110675199hg19UCSC Ensembl
Outerchr13:110672968..110678775hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385808
hg195808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008305, nssv4008306, nssv4008310, nssv4008311, nssv4008304, nssv4008308, nssv4008309, nssv4008307
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154973
Frequency
Sample Size131
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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