A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688358



Internal ID15425010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31859532..31910068hg38UCSC Ensembl
Innerchr12:32012466..32063002hg19UCSC Ensembl
Innerchr12:31903733..31954269hg18UCSC Ensembl
Innerchr12:31903733..31954269hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3850537
hg1950537
hg1850537
hg1750537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516507
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688358
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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