A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525375



Internal ID15105982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77334838..77336864hg38UCSC Ensembl
Innerchr17:75330920..75332946hg19UCSC Ensembl
Innerchr17:72842515..72844541hg18UCSC Ensembl
Innerchr17:72842515..72844541hg17UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg382027
hg192027
hg182027
hg172027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701496
Samples
Known GenesSEPT9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525375
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