A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671462



Internal ID15061428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2650464..3091456hg38UCSC Ensembl
Innerchr10:2692656..3133648hg19UCSC Ensembl
Innerchr10:2682656..3123648hg18UCSC Ensembl
Innerchr10:2682656..3123648hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38440993
hg19440993
hg18440993
hg17440993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517630
Supporting Variants
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671462
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