A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522345



Internal ID15449638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36960768..36961475hg38UCSC Ensembl
Innerchr9:36960765..36961472hg19UCSC Ensembl
Innerchr9:36950765..36951472hg18UCSC Ensembl
Innerchr9:36950765..36951472hg17UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38708
hg19708
hg18708
hg17708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695125
Samples
Known GenesPAX5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522345
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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