A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945319



Internal ID18592170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:224032824..224033676hg38UCSC Ensembl
Innerchr1:224220526..224221378hg19UCSC Ensembl
Innerchr1:222287149..222288001hg18UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38853
hg19853
hg18853
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1819282, nssv1819283, nssv1819280, nssv1819277, nssv1819275, nssv1819279, nssv1819274, nssv1819278, nssv1819276, nssv1819281
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945319
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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