A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156612



Internal ID22087013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143541857..143785200hg38UCSC Ensembl
Outerchr1:143538619..143796140hg38UCSC Ensembl
Innerchr1:149036524..149279840hg19UCSC Ensembl
Outerchr1:149024808..149290775hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38257522
hg19265968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18n97
Supporting Variantsnssv4021026
Samples
Known GenesLOC101929780, LOC388692, NBPF23
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156612
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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