A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156765



Internal ID22087166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156089623..156094352hg38UCSC Ensembl
Outerchr7:156087157..156095374hg38UCSC Ensembl
Innerchr7:155882317..155887046hg19UCSC Ensembl
Outerchr7:155879851..155888068hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg388218
hg198218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021793
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156765
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