A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946155



Internal ID18593005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:114460071..114461877hg38UCSC Ensembl
Innerchr1:115002693..115004499hg19UCSC Ensembl
Innerchr1:114804216..114806022hg18UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381807
hg191807
hg181807
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1783882, nssv1783877, nssv1783880, nssv1783881, nssv1783878, nssv1783885, nssv1783876, nssv1783879, nssv1783883, nssv1783884
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTRIM33
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946155
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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