A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517664



Internal ID15098271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94132981..94179870hg38UCSC Ensembl
Innerchr11:93866147..93913036hg19UCSC Ensembl
Innerchr11:93505795..93552684hg18UCSC Ensembl
Innerchr11:93505795..93552684hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3846890
hg1946890
hg1846890
hg1746890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676732, nssv690793, nssv689662, nssv693488, nssv690033, nssv655683, nssv664725, nssv680736, nssv689570, nssv652761, nssv673392, nssv660324, nssv671466, nssv700440
Samples
Known GenesPANX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517664
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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