A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516241



Internal ID15096848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89696002..89723490hg38UCSC Ensembl
Innerchr16:89762410..89789898hg19UCSC Ensembl
Innerchr16:88289911..88317399hg18UCSC Ensembl
Innerchr16:88289911..88317399hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3827489
hg1927489
hg1827489
hg1727489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667000, nssv691980, nssv683166, nssv681078, nssv657073, nssv655933, nssv691476, nssv683279, nssv676855, nssv674088
Samples
Known GenesCDK10, SPATA2L, VPS9D1, VPS9D1-AS1, ZNF276
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516241
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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