A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011882



Internal ID22073513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7678826..7762163hg38UCSC Ensembl
Outerchr18:7670049..7763365hg38UCSC Ensembl
Innerchr18:7678824..7762161hg19UCSC Ensembl
Outerchr18:7670047..7763363hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3893317
hg1993317
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155500
Supporting Variants
Samples
Known GenesPTPRM
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011882
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