A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528672



Internal ID15455965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126444871..126464913hg38UCSC Ensembl
Innerchr9:129207150..129227192hg19UCSC Ensembl
Innerchr9:128246971..128267013hg18UCSC Ensembl
Innerchr9:126286704..126306746hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3820043
hg1920043
hg1820043
hg1720043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705310
Samples
Known GenesMVB12B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528672
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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