A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656309



Internal ID15392961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176171442..176189554hg38UCSC Ensembl
Innerchr3:175889230..175907342hg19UCSC Ensembl
Innerchr3:177371924..177390036hg18UCSC Ensembl
Innerchr3:177371932..177390044hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3818113
hg1918113
hg1818113
hg1718113
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516429
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656309
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