A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655985



Internal ID15392637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135420547..135469324hg38UCSC Ensembl
Innerchr9:138312393..138361170hg19UCSC Ensembl
Innerchr9:137452214..137500991hg18UCSC Ensembl
Innerchr9:135538338..135587115hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3848778
hg1948778
hg1848778
hg1748778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517428
Supporting Variants
Samples
Known GenesPPP1R26-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655985
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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