A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521136



Internal ID15101743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93020385..93036589hg38UCSC Ensembl
Innerchr9:95782667..95798871hg19UCSC Ensembl
Innerchr9:94822488..94838692hg18UCSC Ensembl
Innerchr9:92862222..92878426hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3816205
hg1916205
hg1816205
hg1716205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695612, nssv693087, nssv682722
Samples
Known GenesFGD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521136
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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