A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680854



Internal ID15417506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:30322957..30332847hg38UCSC Ensembl
Innerchr14:30792163..30802053hg19UCSC Ensembl
Innerchr14:29861914..29871804hg18UCSC Ensembl
Innerchr14:29861914..29871804hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg389891
hg199891
hg189891
hg179891
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517611
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680854
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