A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521594



Internal ID15102201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127263077..127290826hg38UCSC Ensembl
Innerchr9:130025356..130053105hg19UCSC Ensembl
Innerchr9:129065177..129092926hg18UCSC Ensembl
Innerchr9:127104910..127132659hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3827750
hg1927750
hg1827750
hg1727750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698211
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521594
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