A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517195



Internal ID15444488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7238099..7253416hg38UCSC Ensembl
Innerchr5:7238212..7253529hg19UCSC Ensembl
Innerchr5:7291212..7306529hg18UCSC Ensembl
Innerchr5:7291212..7306529hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3815318
hg1915318
hg1815318
hg1715318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653987, nssv671196
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517195
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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