A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945768



Internal ID18245933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11022157..11024068hg38UCSC Ensembl
Innerchr1:11082214..11084125hg19UCSC Ensembl
Innerchr1:11004801..11006712hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381912
hg191912
hg181912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1754928, nssv1754934, nssv1754931, nssv1754927, nssv1754932, nssv1754926, nssv1754933, nssv1754930, nssv1754935, nssv1754929
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTARDBP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945768
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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