A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975379



Internal ID18610587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39331632..39350249hg38UCSC Ensembl
Innerchr11:39353182..39371799hg19UCSC Ensembl
Innerchr11:39309758..39328375hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3818618
hg1918618
hg1818618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757407
SamplesHGDP01284
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975379
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