A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945309



Internal ID18245497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:222668625..222670424hg38UCSC Ensembl
Innerchr1:222841967..222843766hg19UCSC Ensembl
Innerchr1:220908590..220910389hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381800
hg191800
hg181800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1819803, nssv1819799, nssv1818870, nssv1819798, nssv1819800, nssv1819802, nssv1819797, nssv1819801, nssv1819796, nssv1818871
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAIDA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945309
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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