A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525053



Internal ID15105660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127251022..127271936hg38UCSC Ensembl
Innerchr9:130013301..130034215hg19UCSC Ensembl
Innerchr9:129053122..129074036hg18UCSC Ensembl
Innerchr9:127092855..127113769hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3820915
hg1920915
hg1820915
hg1720915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701101
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525053
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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