A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672197



Internal ID15408849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:107648275..107692283hg38UCSC Ensembl
Innerchr8:108660503..108704511hg19UCSC Ensembl
Innerchr8:108729679..108773687hg18UCSC Ensembl
Innerchr8:108729679..108773687hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3844009
hg1944009
hg1844009
hg1744009
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516660
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672197
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