A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011962



Internal ID22073593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61388158..61396537hg38UCSC Ensembl
Outerchr18:61387179..61400110hg38UCSC Ensembl
Innerchr18:59055391..59063770hg19UCSC Ensembl
Outerchr18:59054412..59067343hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3812932
hg1912932
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155522
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011962
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