A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702307



Internal ID15438959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85829000..85867136hg38UCSC Ensembl
Innerchr6:86538718..86576854hg19UCSC Ensembl
Innerchr6:86595437..86633573hg18UCSC Ensembl
Innerchr6:86595437..86633573hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3838137
hg1938137
hg1838137
hg1738137
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526067
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702307
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