A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156789



Internal ID22087190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158292410..158301746hg38UCSC Ensembl
Outerchr1:158290342..158309227hg38UCSC Ensembl
Innerchr1:158262200..158271536hg19UCSC Ensembl
Outerchr1:158260132..158279017hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3818886
hg1918886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022959
Samples
Known GenesCD1C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156789
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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