A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528325



Internal ID15455618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8048501..8051047hg38UCSC Ensembl
Innerchr17:7951819..7954365hg19UCSC Ensembl
Innerchr17:7892544..7895090hg18UCSC Ensembl
Innerchr17:7892544..7895090hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382547
hg192547
hg182547
hg172547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704906
Samples
Known GenesALOX15B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528325
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