A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156626



Internal ID22087027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2296386..2529136hg38UCSC Ensembl
Outerchr7:2294751..2538030hg38UCSC Ensembl
Innerchr7:2336021..2568770hg19UCSC Ensembl
Outerchr7:2334386..2577664hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38243280
hg19243279
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4023019
Samples
Known GenesBRAT1, CHST12, EIF3B, LFNG, LOC101927181, MIR4648, SNX8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156626
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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