A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156706



Internal ID22087107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103197500..103228563hg38UCSC Ensembl
Outerchr7:103188138..103237281hg38UCSC Ensembl
Innerchr7:102837947..102869010hg19UCSC Ensembl
Outerchr7:102828585..102877728hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3849144
hg1949144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv267n97
Supporting Variantsnssv4022210
Samples
Known GenesDPY19L2P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156706
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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