A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967241



Internal ID18255783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77620480..77623843hg38UCSC Ensembl
Innerchr3:77669631..77672994hg19UCSC Ensembl
Innerchr3:77752321..77755684hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg383364
hg193364
hg183364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2766647
SamplesHGDP00998
Known GenesROBO2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967241
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