A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983744



Internal ID18618937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103330532..103346342hg38UCSC Ensembl
Innerchr13:103982882..103998692hg19UCSC Ensembl
Innerchr13:102780883..102796693hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3815811
hg1915811
hg1815811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2760949
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983744
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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