A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528600



Internal ID15109207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36137349..36173151hg38UCSC Ensembl
Innerchr9:36137346..36173148hg19UCSC Ensembl
Innerchr9:36127346..36163148hg18UCSC Ensembl
Innerchr9:36127346..36163148hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3835803
hg1935803
hg1835803
hg1735803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705226
Samples
Known GenesCCIN, GLIPR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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