A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975804



Internal ID18264325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122833633..122836634hg38UCSC Ensembl
Innerchr10:124593149..124596150hg19UCSC Ensembl
Innerchr10:124583139..124586140hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383002
hg193002
hg183002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761943
SamplesHGDP00998
Known GenesCUZD1, FAM24B-CUZD1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975804
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