A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701988



Internal ID15091954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77188498..77202141hg38UCSC Ensembl
Innerchr3:77237649..77251292hg19UCSC Ensembl
Innerchr3:77320339..77333982hg18UCSC Ensembl
Innerchr3:77320339..77333982hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3813644
hg1913644
hg1813644
hg1713644
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525804
Supporting Variants
Samples
Known GenesROBO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701988
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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