A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528719



Internal ID15456012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126610956..126644710hg38UCSC Ensembl
Innerchr9:129373235..129406989hg19UCSC Ensembl
Innerchr9:128413056..128446810hg18UCSC Ensembl
Innerchr9:126452789..126486543hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3833755
hg1933755
hg1833755
hg1733755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705369
Samples
Known GenesLMX1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528719
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