A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673058



Internal ID15409710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101187290..101589980hg38UCSC Ensembl
Innerchr5:100522994..100925684hg19UCSC Ensembl
Innerchr5:100550893..100953583hg18UCSC Ensembl
Innerchr5:100550893..100953583hg17UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38402691
hg19402691
hg18402691
hg17402691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516292
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673058
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