A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517655



Internal ID15444948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:74639418..74649630hg38UCSC Ensembl
Innerchr9:77254334..77264546hg19UCSC Ensembl
Innerchr9:76444154..76454366hg18UCSC Ensembl
Innerchr9:74483888..74494100hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810213
hg1910213
hg1810213
hg1710213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689532, nssv652681
Samples
Known GenesRORB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517655
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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