A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156702



Internal ID22087103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99194455..99199831hg38UCSC Ensembl
Outerchr7:99190613..99201035hg38UCSC Ensembl
Innerchr7:98792078..98797454hg19UCSC Ensembl
Outerchr7:98788236..98798658hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3810423
hg1910423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022201
Samples
Known GenesKPNA7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156702
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer