A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517635



Internal ID15444928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:31890473..31902059hg38UCSC Ensembl
Innerchr20:30478276..30489862hg19UCSC Ensembl
Innerchr20:29941937..29953523hg18UCSC Ensembl
Innerchr20:29941937..29953523hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3811587
hg1911587
hg1811587
hg1711587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686876, nssv681379, nssv690074, nssv689761, nssv682540, nssv680087, nssv663173, nssv666155, nssv659613, nssv680714, nssv684440, nssv686164, nssv688796, nssv679803, nssv660836, nssv664855, nssv652629, nssv682885, nssv677923, nssv656705, nssv693940, nssv666210, nssv673678, nssv658825, nssv673713, nssv654671, nssv688452, nssv661413, nssv679714, nssv691064, nssv675940, nssv667406, nssv670613, nssv671445, nssv668015
Samples
Known GenesTTLL9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517635
Frequency
Sample Size2026
Observed Gain35
Observed Loss0
Observed Complex0
Frequencyn/a


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