A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515747



Internal ID15442804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4501492..4502575hg38UCSC Ensembl
Innerchr9:4501492..4502575hg19UCSC Ensembl
Innerchr9:4491492..4492575hg18UCSC Ensembl
Innerchr9:4491492..4492575hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381084
hg191084
hg181084
hg171084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667457, nssv678526, nssv674041, nssv664665, nssv671317, nssv669880, nssv660317, nssv676226, nssv675805, nssv673699, nssv684727, nssv685859, nssv691930
Samples
Known GenesSLC1A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515747
Frequency
Sample Size2026
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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