A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156708



Internal ID22087109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106486066..106492205hg38UCSC Ensembl
Outerchr7:106481995..106497952hg38UCSC Ensembl
Innerchr7:106126512..106132651hg19UCSC Ensembl
Outerchr7:106122441..106138398hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3815958
hg1915958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022212
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156708
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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