A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527574



Internal ID15454867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:119319540..119328192hg38UCSC Ensembl
Innerchr9:122081818..122090470hg19UCSC Ensembl
Innerchr9:121121639..121130291hg18UCSC Ensembl
Innerchr9:119161372..119170024hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg388653
hg198653
hg188653
hg178653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704035
Samples
Known GenesBRINP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527574
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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