A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527633



Internal ID15454926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8295843..8313419hg38UCSC Ensembl
Innerchr17:8199161..8216737hg19UCSC Ensembl
Innerchr17:8139886..8157462hg18UCSC Ensembl
Innerchr17:8139886..8157462hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3817577
hg1917577
hg1817577
hg1717577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704102
Samples
Known GenesARHGEF15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527633
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