A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155491



Internal ID22085996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61848230..61853874hg38UCSC Ensembl
Outerchr17:61835797..61855832hg38UCSC Ensembl
Innerchr17:59925591..59931235hg19UCSC Ensembl
Outerchr17:59913158..59933193hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3820036
hg1920036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011871
Samples
Known GenesBRIP1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155491
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