A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516752



Internal ID15444045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5267043..5345673hg38UCSC Ensembl
Innerchr9:5267043..5345673hg19UCSC Ensembl
Innerchr9:5257043..5335673hg18UCSC Ensembl
Innerchr9:5257043..5335673hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3878631
hg1978631
hg1878631
hg1778631
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663769, nssv662692, nssv691005, nssv667458, nssv683252, nssv705911, nssv661863, nssv674580, nssv678781, nssv666665, nssv693620, nssv663257, nssv687856, nssv694047, nssv668467, nssv669698, nssv670702, nssv654420, nssv659409, nssv653758, nssv661774, nssv686194, nssv657676, nssv689053, nssv660662, nssv692662, nssv673365, nssv693024, nssv653442, nssv663716, nssv678640, nssv667259, nssv693086
Samples
Known GenesRLN1, RLN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516752
Frequency
Sample Size2026
Observed Gain9
Observed Loss24
Observed Complex0
Frequencyn/a


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