A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975221



Internal ID18610429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102230845..102231942hg38UCSC Ensembl
Innerchr11:102101576..102102673hg19UCSC Ensembl
Innerchr11:101606786..101607883hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381098
hg191098
hg181098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1902470, nssv1902469, nssv1902467, nssv1902471, nssv1902468, nssv1902473, nssv1902472, nssv1902465, nssv1902464, nssv1902466
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesYAP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975221
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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