A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2018351



Internal ID17438704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32610794..32632860hg38UCSC Ensembl
Innerchr15:32902995..32925061hg19UCSC Ensembl
Innerchr15:30690287..30712353hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3822067
hg1922067
hg1822067
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv977696
Supporting Variants
SamplesHGDP00665
Known GenesARHGAP11A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2018351
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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