A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156479



Internal ID22086880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109700332..109703659hg38UCSC Ensembl
Outerchr1:109697556..109707613hg38UCSC Ensembl
Innerchr1:110242954..110246281hg19UCSC Ensembl
Outerchr1:110240178..110250235hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810058
hg1910058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv15n97
Supporting Variantsnssv4020428, nssv4020426, nssv4020427, nssv4020431, nssv4020429, nssv4020430
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156479
Frequency
Sample Size131
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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